Trials / Completed
CompletedNCT00996489
This is a Post Approval Study of Coaptite® in the Treatment of Female Urinary Incontinence
Post-approval of Coaptite® in the Treatment of Female Urinary Incontinence
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 459 (actual)
- Sponsor
- Merz North America, Inc. · Industry
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a post approval study of Coaptite® in the treatment of female urinary incontinence.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Coaptite® | Calcium hydroxylapatite particles suspended in an aqueous based gel carrier |
Timeline
- Start date
- 2008-01-08
- Primary completion
- 2015-10-26
- Completion
- 2015-11-02
- First posted
- 2009-10-16
- Last updated
- 2019-07-23
- Results posted
- 2019-07-23
Locations
20 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00996489. Inclusion in this directory is not an endorsement.