Clinical trial
Adjustable Continence Therapy (ACT) Device for the Treatment of Female Stress…
NCT00113555 · Uromedica, Industry · Completed
Key facts
| NCT number | NCT00113555 |
|---|---|
| Title | Adjustable Continence Therapy (ACT) Device for the Treatment of Female Stress Urinary Incontinence |
| Official title | Clinical Investigation of an Adjustable Continence Therapy (ACT) Periurethral Prosthetic System for Treatment of Female Stress Urinary Incontinence With or Without Hypermobility |
| Acronym | ACT |
| Lead sponsor | Uromedica, Industry |
| Status | Completed |
| Study type | Interventional |
| Conditions | Urinary Incontinence |
| Intervention type | Device |
| Interventions | ACT (Adjustable Continence Therapy) |
| Enrollment | 221 |
| Start date | Dec 1, 2001 |
| Primary completion | Jul 1, 2008 |
| Completion | Nov 1, 2010 |
| First posted | Jun 9, 2005 |
| Last update posted | Jul 9, 2018 |
| Countries | Canada, United States |
At a glance
- 1–9 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: