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One site still open but on hold due to financial issues. Enrollment will resume once payments are started up again. Other sites closed.
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This trial is to assess the safety and clinical performance of Contino device is preventing Urinary Incontinence in male subjects with Sphincteric Incompetence
Sphincteric incompetence is most commonly found in men who have had radical prostatectomy (RP). RP is the most common treatment for localized high-risk Prostate Cancer in North America.
The Contino®, a urethral insert, was conceived by a prostate cancer survivor and worn for 10+ years without incident, and a First in Human clinical trial was completed without serious adverse event. The basis for this clinical trial is a post market clinical follow-up study. No drug treatment will be administered.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Device Use | Experimental | Only one arm |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Contino | Device | The Contino® urethral insert is a self-administered licensed medical device, is inserted into the distal portion of the male urethra inhibiting the flow of urine. The Contino is self-inserted into the adult male urethra and is removed prior to urination. Much more than just a device, Contino® is an integrated solution that includes personalised fitting and support from incontinence specialists. It is made from highly specialised medical grade polymer, which has been extensively tested for biocompatibility. |
| Measure | Description | Time Frame |
|---|---|---|
| To establish the safety of the Contino® | safety is characterized by the absence of complications | 14 Months |
| To establish the clinical performance of the Contino® | Clinical performance is characterized by the ability to stop involuntary urine flow | 14 Months |
| Change from baseline in the ICIQ-SF score | At Visit Days 30 and 60 | 14 Months |
| Change from baseline in the weight of the protective pads | At Visit Days 30 and 60 | 14 Months |
| Measure | Description | Time Frame |
|---|---|---|
| Level of ease of use inserting the Contino® from the Follow-up Questionnaire | Level of comfort measurement | 14 Months |
| Level of ease of use removing the Contino® from the Follow-up Questionnaire |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Dean Elterman, MD | University Urology Associates | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| The Fe/Male Health Centres | Oakville | Ontario | L6H 3P1 | Canada | ||
| Dr. Dean Elterman |
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| ID | Term |
|---|---|
| D014549 | Urinary Incontinence |
| ID | Term |
|---|---|
| D014555 | Urination Disorders |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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|
Level of comfort measurement
| 14 Months |
| Number of subjects with newly observed urinary function improvements | including (but not limited to): being able to urinate independently for the first time since prostate surgery, return of urge to void and sensation of full bladder, better urinary stream, reduced time urinating from the follow up questionnaire | 14 Months |
| Toronto |
| Ontario |
| M5G 1E2 |
| Canada |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D059411 | Lower Urinary Tract Symptoms |
| D020924 | Urological Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |