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The purpose of the investigational device in the proposed clinical investigation is to capture pressure data prior to and during voiding using a CE-marked commercially available catheter.
This clinical investigation is based on an open explorative design evaluating the sensor ability to record readable data in healthy volunteers and the extent of artifacts influencing data quality and readability in healthy volunteers.
Overall:
Duration:
Information visit:
Oral and written information about the evaluation is given by the PI or his/her representative. Subjects can continue to visit 0, inclusion visit, the same day - if the subject has decided on participation and if practically possible.
Visit 0 - Inclusion visit:
Informed consent signed. Subjects can continue to visit 1 - test visit the same day - if practically possible.
Visit 1 - test visit:
1h test visit at Rigshospitalet. Fertile females will be asked to perform a pregnancy test. Subject is asked about symptoms for urinary tract infections (frequent urination, stinging or pain at urination). If negative for these symptoms, the subject will be catheterised with (SpeediCath® Standard, male/female, Nelaton tip depending of the gender) with fitted pressure sensor. The urine is led into a standard urine flowmeter.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| IC connected to a sensor | Experimental | Single use of a IC connected to a sensor |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| SpeediCath(R) | Device | IC SpeediCath ® connected to pressure sensor |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Readability of Pressure Sensor Measurements | Determination of whether the sensor could detect changes in pressure in kilopascal (kPa) and provide a readable graph depicting changes in kPa over time of use of IC. Each pressure sensor graph is assessed visually to determine whether the instrument can be used in future studies on a Yes/No basis. The total number of participants with readable pressure sensor measurements were counted. | 1 hour |
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Inclusion Criteria:
Exclusion Criteria:
at least 4 of each gender
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| Name | Affiliation | Role |
|---|---|---|
| Fredrik Ceder, M.Sc | Head of Clinical Operations | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Urology | Copenhagen | 2100 | Denmark |
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| ID | Title | Description |
|---|---|---|
| FG000 | Participants Undergoing Catheterization With SpeediCath ® | One time use of intermittent catheterization with SpeediCath ® connected to a pressure sensor for 8 males and 4 females |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
One time use of intermittent catheterization with SpeediCath ® connected to a pressure sensor for 8 males and 4 females
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| ID | Title | Description |
|---|---|---|
| BG000 | Participants Undergoing Catheterization With SpeediCath ® | One time use of intermittent catheterization with SpeediCath ® connected to a pressure sensor for 8 males and 4 females |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| 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 | Number of Participants With Readability of Pressure Sensor Measurements | Determination of whether the sensor could detect changes in pressure in kilopascal (kPa) and provide a readable graph depicting changes in kPa over time of use of IC. Each pressure sensor graph is assessed visually to determine whether the instrument can be used in future studies on a Yes/No basis. The total number of participants with readable pressure sensor measurements were counted. | Posted | Count of Participants | Participants | 1 hour |
|
1 hour
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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 | Participants Undergoing Catheterization With SpeediCath ® | One time use of intermittent catheterization with SpeediCath ® connected to a pressure sensor for 8 males and 4 females |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Vice President, Medical Affairs | Coloplast | +45 4911 1111 | clinical-studies@coloplast.com |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Aug 30, 2019 | Jan 31, 2020 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D010349 | Patient Compliance |
| ID | Term |
|---|---|
| D010342 | Patient Acceptance of Health Care |
| D000074822 | Treatment Adherence and Compliance |
| D015438 | Health Behavior |
| D001519 | Behavior |
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Single arm - open-label study
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| Participants |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Units |
|---|
| Counts |
|---|
| Participants |
|
|
| 0 |
| 12 |
| 0 |
| 12 |
| 0 |
| 12 |
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