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Sponsor decision
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The purpose of this study is to evaluate the safety and performance of the ProstaCare System in relieving symptoms of urinary outflow obstruction secondary to benign prostatic hyperplasia.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment | Other |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| prostaFix System | Device |
|
| Measure | Description | Time Frame |
|---|---|---|
| Mean International Prostate Symptom Score (IPSS) at 3 Months Follow-up Visit | The primary effectiveness objective was to demonstrate that mean IPSS improvement (Δ IPSS) following treatment with the prostaFix System exceeded 6.5 points with 95% confidence 3 months after treatment. The International Prostate Symptom Score (IPSS) is a validated questionnaire used to assess baseline and post treatment BPH symptoms. It is based on the answers to seven questions concerning urinary symptoms and one question concerning quality of life. Each question concerning urinary symptoms allows the subject to choose one out of six answers indicating increasing severity of that particular symptom. The answers are assigned points from 0 to 5. The total score can therefore range from 0 to 35 (asymptomatic to very symptomatic): Mild (symptom score less than or equal to 7), Moderate (symptom score range 8-19) and Severe (symptom score range 20-35). Improvement in BPH symptoms is seen as a decrease in IPSS. | 3 months after treatment |
| Number of Participants With Serious Adverse Events (SAEs) | The primary safety objective of this study was to estimate the proportion of subjects affected by serious adverse events (SAEs) associated with the use of the device. This objective was addressed through recording all adverse events (AEs) observed or reported during the course of the study. | 3 months after treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Mean Change in QOL From Baseline | Question eight of the IPSS questionnaire refers to the subject's perceived quality of life (QOL). The International Scientific Committee (SCI), under the patronage of the World Health Organization (WHO) and the International Union Against Cancer (UICC), recommends the use of only a single question to assess the quality of life. The answers to this question range from "delighted" to "terrible" or 0 to 6. |
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Key Inclusion Criteria:
Key Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Henry Ho Sun Sien, MD | Singapore General Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Urology Bay of Plenty (BOP) | Tauranga | 3112 | New Zealand | |||
| National University Hospital |
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| ID | Title | Description |
|---|---|---|
| FG000 | prostaFix System | Subjects treated with the prostaFix Water Electrolysis System |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
All subjects who enrolled in the study and were treated with the prostaFix System.
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| ID | Title | Description |
|---|---|---|
| BG000 | Treatment | Subjects treated with the prostaFix System |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Mean International Prostate Symptom Score (IPSS) at 3 Months Follow-up Visit | The primary effectiveness objective was to demonstrate that mean IPSS improvement (Δ IPSS) following treatment with the prostaFix System exceeded 6.5 points with 95% confidence 3 months after treatment. The International Prostate Symptom Score (IPSS) is a validated questionnaire used to assess baseline and post treatment BPH symptoms. It is based on the answers to seven questions concerning urinary symptoms and one question concerning quality of life. Each question concerning urinary symptoms allows the subject to choose one out of six answers indicating increasing severity of that particular symptom. The answers are assigned points from 0 to 5. The total score can therefore range from 0 to 35 (asymptomatic to very symptomatic): Mild (symptom score less than or equal to 7), Moderate (symptom score range 8-19) and Severe (symptom score range 20-35). Improvement in BPH symptoms is seen as a decrease in IPSS. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | 3 months after treatment |
Adverse events were collected from enrollment until study termination. All enrolled subjects were followed to at least their 12-month follow-up visit.
AEs were classified by the investigator at each corresponding site for relatedness to the device and seriousness based on the Common Terminology Criteria for Adverse Events (Version 4.03) (CTCAE) (US Department of Health and Human Services 2010) guidelines. In addition, the adverse events were coded using MedDRA and reviewed by the Medical Advisor.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | prostaFix System | Subjects treated with the prostaFix Water Electrolysis System |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Haematuria | Renal and urinary disorders | MedDRA 10.0 | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Back Pain | Musculoskeletal and connective tissue disorders | MedDRA 10.0 | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Annegret Genger | seleon gmbh | +49 175 934 91 83 | Annegret.Genger@seleon.de |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Jan 1, 2018 | Aug 3, 2021 | Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Nov 6, 2018 | Aug 3, 2021 | SAP_001.pdf |
Not provided
| ID | Term |
|---|---|
| D011470 | Prostatic Hyperplasia |
| ID | Term |
|---|---|
| D011469 | Prostatic Diseases |
| D005832 | Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
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| Baseline and 3 months after treatment |
| Mean Change in Peak Flow Rate (Qmax) From Baseline | Uroflowmetry measures the flow of urine. It tracks how fast urine flows (peak flow rate - Qmax), how much flows out, and how long it takes. It's a diagnostic test to assess how well the urinary tract functions. Uroflowmetry is used in BPH subjects to help the doctors determine how well the subject's urinary tract is doing and the severity of obstruction caused by the prostate. The higher the Qmax is, the less obstructed the urethra. | Baseline and 3 months after treatment |
| Mean Change in Post Void Residual (PVR) From Baseline | The Post Void Residual (PVR) is an indicator of urine remaining in the bladder after voiding. A healthy bladder should be fairly empty following urination. A volume < 50 mL is normal; < 100 mL is usually acceptable in patients > 65 years old. The higher the PVR, the more urine is left in the bladder and this can be seen as a sign of increased obstruction of the urethra. | Baseline and 3 months after treatment |
| Mean Change in MSHQ-EjD Score From Baseline | The MSHQ-EjD Short Form (Male Sexual Health Questionnaire - Ejaculatory Disfunction) is composed of three questions that rate ejaculatory function in men. A fourth question measures the MSHQ-EjD Bother, this asks the subject if he is bothered by his level of ejaculatory function. MSHQ-EjD total score ranges from 1 to 15 with a higher score indicating better sexual functioning. MSHQ-EjD bother score ranges from 0 to 5 with a higher score indicating greater bother. An increase in the MSHQ-EjD Total Score indicates better ejaculation and a decrease in the MSHQ-EjD Bother Score means that the subject is less bothered by his ejaculatory function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Baseline and 3 months after treatment |
| Change in IIEF Score From Baseline | The IIEF (International Index of Erectile Function) provides a broad measure of sexual function; an increase in score indicates an improvement in sexual function. This questionnaire consists of five questions that asks the subject of any erection problems that have impacted his sexual life over the past 4 weeks or since the last study visit, whichever is shorter. IIEF total score ranges from 0 to 25 with a higher score indicating better sexual functioning and an increase in score indicates an improvement in sexual function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Baseline and 3 months after treatment |
| Mean Change in IPSS From Baseline | The International Prostate Symptom Score (IPSS) is a validated questionnaire used to assess baseline and post treatment BPH symptoms. It is based on the answers to seven questions concerning urinary symptoms and one question concerning quality of life. Each question concerning urinary symptoms allows the subject to choose one out of six answers indicating increasing severity of that particular symptom. The answers are assigned points from 0 to 5. The total score can therefore range from 0 to 35 (asymptomatic to very symptomatic): Mild (symptom score less than or equal to 7), Moderate (symptom score range 8-19) and Severe (symptom score range 20-35). Improvement in BPH symptoms is seen as a decrease in IPSS. | Baseline and 12 months from treatment |
| Mean Change in QOL From Baseline | Question eight of the IPSS questionnaire refers to the subject's perceived quality of life (QOL). The International Scientific Committee (SCI), under the patronage of the World Health Organization (WHO) and the International Union Against Cancer (UICC), recommends the use of only a single question to assess the quality of life. The answers to this question range from "delighted" to "terrible" or 0 to 6. | Baseline and 12 months from treatment |
| Mean Change in Peak Flow Rate (Qmax) From Baseline | Uroflowmetry measures the flow of urine. It tracks how fast urine flows (peak flow rate - Qmax), how much flows out, and how long it takes. It's a diagnostic test to assess how well the urinary tract functions. Uroflowmetry is used in BPH subjects to help the doctors determine how well the subject's urinary tract is doing and the severity of obstruction caused by the prostate. The higher the Qmax is, the less obstructed the urethra. | Baseline and 12 months from treatment |
| Mean Change in Post Void Residual (PVR) From Baseline | The Post Void Residual (PVR) is an indicator of urine remaining in the bladder after voiding. A healthy bladder should be fairly empty following urination. A volume < 50 mL is normal; < 100 mL is usually acceptable in patients > 65 years old. The higher the PVR, the more urine is left in the bladder and this can be seen as a sign of increased obstruction of the urethra. | Baseline and 12 months from treatment |
| Mean Change in MSHQ-EjD From Baseline | The MSHQ-EjD Short Form (Male Sexual Health Questionnaire - Ejaculatory Disfunction) is composed of three questions that rate ejaculatory function in men. A fourth question measures the MSHQ-EjD Bother, this asks the subject if he is bothered by his level of ejaculatory function. MSHQ-EjD total score ranges from 1 to 15 with a higher score indicating better sexual functioning. MSHQ-EjD bother score ranges from 0 to 5 with a higher score indicating greater bother. An increase in the MSHQ-EjD Total Score indicates better ejaculation and a decrease in the MSHQ-EjD Bother Score means that the subject is less bothered by his ejaculatory function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Baseline and 12 months from treatment |
| Mean Change in IIEF From Baseline | The IIEF (International Index of Erectile Function) provides a broad measure of sexual function; an increase in score indicates an improvement in sexual function. This questionnaire consists of five questions that asks the subject of any erection problems that have impacted his sexual life over the past 4 weeks or since the last study visit, whichever is shorter. IIEF total score ranges from 0 to 25 with a higher score indicating better sexual functioning and an increase in score indicates an improvement in sexual function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Baseline and 12 months from treatment |
| MRI Necrosis Volume | The prostaFix System uses pH shifts induced by water electrolysis to induce necrosis in the hyperplastic prostate tissue. The induced necrosis within the borders of the prostate result in a pressure reduction and thereby relieve the symptoms of BPH. This necrosis that resulted from the procedure eventually heals and necrosis volume should reduce overtime. Per protocol, only the first 10-15 subjects would have MRI studies at done to assess subject safety and treatment effect. then MRI was optional. A total of 14 subjects actually had an MRI and the results are reported for those subjects. | 3 months after treatment |
| Singapore |
| 119074 |
| Singapore |
| Singapore General Hospital | Singapore | 169608 | Singapore |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race/Ethnicity, Customized | Count of Participants | Participants |
|
| Region of Enrollment | Count of Participants | Participants |
|
| ID | Title | Description |
|---|---|---|
| OG000 | prostaFix System | Subjects treated with the prostaFix Water Electrolysis System |
|
|
|
| Primary | Number of Participants With Serious Adverse Events (SAEs) | The primary safety objective of this study was to estimate the proportion of subjects affected by serious adverse events (SAEs) associated with the use of the device. This objective was addressed through recording all adverse events (AEs) observed or reported during the course of the study. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Count of Participants | Participants | No | 3 months after treatment |
|
|
|
| Secondary | Mean Change in QOL From Baseline | Question eight of the IPSS questionnaire refers to the subject's perceived quality of life (QOL). The International Scientific Committee (SCI), under the patronage of the World Health Organization (WHO) and the International Union Against Cancer (UICC), recommends the use of only a single question to assess the quality of life. The answers to this question range from "delighted" to "terrible" or 0 to 6. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | Baseline and 3 months after treatment |
|
|
|
| Secondary | Mean Change in Peak Flow Rate (Qmax) From Baseline | Uroflowmetry measures the flow of urine. It tracks how fast urine flows (peak flow rate - Qmax), how much flows out, and how long it takes. It's a diagnostic test to assess how well the urinary tract functions. Uroflowmetry is used in BPH subjects to help the doctors determine how well the subject's urinary tract is doing and the severity of obstruction caused by the prostate. The higher the Qmax is, the less obstructed the urethra. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | ml/sec | Baseline and 3 months after treatment |
|
|
|
| Secondary | Mean Change in Post Void Residual (PVR) From Baseline | The Post Void Residual (PVR) is an indicator of urine remaining in the bladder after voiding. A healthy bladder should be fairly empty following urination. A volume < 50 mL is normal; < 100 mL is usually acceptable in patients > 65 years old. The higher the PVR, the more urine is left in the bladder and this can be seen as a sign of increased obstruction of the urethra. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | ml | Baseline and 3 months after treatment |
|
|
|
| Secondary | Mean Change in MSHQ-EjD Score From Baseline | The MSHQ-EjD Short Form (Male Sexual Health Questionnaire - Ejaculatory Disfunction) is composed of three questions that rate ejaculatory function in men. A fourth question measures the MSHQ-EjD Bother, this asks the subject if he is bothered by his level of ejaculatory function. MSHQ-EjD total score ranges from 1 to 15 with a higher score indicating better sexual functioning. MSHQ-EjD bother score ranges from 0 to 5 with a higher score indicating greater bother. An increase in the MSHQ-EjD Total Score indicates better ejaculation and a decrease in the MSHQ-EjD Bother Score means that the subject is less bothered by his ejaculatory function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | Baseline and 3 months after treatment |
|
|
|
| Secondary | Change in IIEF Score From Baseline | The IIEF (International Index of Erectile Function) provides a broad measure of sexual function; an increase in score indicates an improvement in sexual function. This questionnaire consists of five questions that asks the subject of any erection problems that have impacted his sexual life over the past 4 weeks or since the last study visit, whichever is shorter. IIEF total score ranges from 0 to 25 with a higher score indicating better sexual functioning and an increase in score indicates an improvement in sexual function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | Baseline and 3 months after treatment |
|
|
|
| Secondary | Mean Change in IPSS From Baseline | The International Prostate Symptom Score (IPSS) is a validated questionnaire used to assess baseline and post treatment BPH symptoms. It is based on the answers to seven questions concerning urinary symptoms and one question concerning quality of life. Each question concerning urinary symptoms allows the subject to choose one out of six answers indicating increasing severity of that particular symptom. The answers are assigned points from 0 to 5. The total score can therefore range from 0 to 35 (asymptomatic to very symptomatic): Mild (symptom score less than or equal to 7), Moderate (symptom score range 8-19) and Severe (symptom score range 20-35). Improvement in BPH symptoms is seen as a decrease in IPSS. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | Baseline and 12 months from treatment |
|
|
|
| Secondary | Mean Change in QOL From Baseline | Question eight of the IPSS questionnaire refers to the subject's perceived quality of life (QOL). The International Scientific Committee (SCI), under the patronage of the World Health Organization (WHO) and the International Union Against Cancer (UICC), recommends the use of only a single question to assess the quality of life. The answers to this question range from "delighted" to "terrible" or 0 to 6. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | Baseline and 12 months from treatment |
|
|
|
| Secondary | Mean Change in Peak Flow Rate (Qmax) From Baseline | Uroflowmetry measures the flow of urine. It tracks how fast urine flows (peak flow rate - Qmax), how much flows out, and how long it takes. It's a diagnostic test to assess how well the urinary tract functions. Uroflowmetry is used in BPH subjects to help the doctors determine how well the subject's urinary tract is doing and the severity of obstruction caused by the prostate. The higher the Qmax is, the less obstructed the urethra. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | ml/sec | Baseline and 12 months from treatment |
|
|
|
| Secondary | Mean Change in Post Void Residual (PVR) From Baseline | The Post Void Residual (PVR) is an indicator of urine remaining in the bladder after voiding. A healthy bladder should be fairly empty following urination. A volume < 50 mL is normal; < 100 mL is usually acceptable in patients > 65 years old. The higher the PVR, the more urine is left in the bladder and this can be seen as a sign of increased obstruction of the urethra. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | ml | Baseline and 12 months from treatment |
|
|
|
| Secondary | Mean Change in MSHQ-EjD From Baseline | The MSHQ-EjD Short Form (Male Sexual Health Questionnaire - Ejaculatory Disfunction) is composed of three questions that rate ejaculatory function in men. A fourth question measures the MSHQ-EjD Bother, this asks the subject if he is bothered by his level of ejaculatory function. MSHQ-EjD total score ranges from 1 to 15 with a higher score indicating better sexual functioning. MSHQ-EjD bother score ranges from 0 to 5 with a higher score indicating greater bother. An increase in the MSHQ-EjD Total Score indicates better ejaculation and a decrease in the MSHQ-EjD Bother Score means that the subject is less bothered by his ejaculatory function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | Baseline and 12 months from treatment |
|
|
|
| Secondary | Mean Change in IIEF From Baseline | The IIEF (International Index of Erectile Function) provides a broad measure of sexual function; an increase in score indicates an improvement in sexual function. This questionnaire consists of five questions that asks the subject of any erection problems that have impacted his sexual life over the past 4 weeks or since the last study visit, whichever is shorter. IIEF total score ranges from 0 to 25 with a higher score indicating better sexual functioning and an increase in score indicates an improvement in sexual function. Due to the sensitive nature of the questions, this questionnaire is voluntary and not all subjects completed it at baseline. Some subjects completed at baseline but decided not to complete at certain follow-up visits which explains the different number of participants during various analysis time frames. | Intent-to-treat (ITT) with last observation carried forward (LOCF): All subjects who enrolled in the study, were treated with the prostaFix System, and completed the 3 month follow-up visit without significant protocol deviations. | Posted | Mean | Standard Error | score on a scale | Baseline and 12 months from treatment |
|
|
|
| Secondary | MRI Necrosis Volume | The prostaFix System uses pH shifts induced by water electrolysis to induce necrosis in the hyperplastic prostate tissue. The induced necrosis within the borders of the prostate result in a pressure reduction and thereby relieve the symptoms of BPH. This necrosis that resulted from the procedure eventually heals and necrosis volume should reduce overtime. Per protocol, only the first 10-15 subjects would have MRI studies at done to assess subject safety and treatment effect. then MRI was optional. A total of 14 subjects actually had an MRI and the results are reported for those subjects. | Posted | Mean | Standard Deviation | cm^3 | 3 months after treatment |
|
|
|
| 0 |
| 46 |
| 3 |
| 46 |
| 24 |
| 46 |
| Haemorrhage (secondary) | Surgical and medical procedures | MedDRA 10.0 | Systematic Assessment |
|
| Urinary Tract Infection | Renal and urinary disorders | MedDRA 10.0 | Systematic Assessment |
|
| Traumatic brain injury | Injury, poisoning and procedural complications | MedDRA 10.0 | Systematic Assessment |
|
| Hypertonic bladder | Renal and urinary disorders | MedDRA 10.0 | Systematic Assessment |
|
| Lower urinary tract symptoms (worsened) | Renal and urinary disorders | MedDRA 10.0 | Systematic Assessment |
|
| Urinary retention | Renal and urinary disorders | MedDRA 10.0 | Systematic Assessment |
|
| Urinary urgency | Renal and urinary disorders | MedDRA 10.0 | Systematic Assessment |
|
Not provided
| D052801 |
| Male Urogenital Diseases |
|
|