Trials / Completed
CompletedNCT01770691
Preliminary Performance Study of the New TIPI Device in the Prevention of Stress Urinary Incontinence
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 7 (actual)
- Sponsor
- Assuta Hospital Systems · Academic / Other
- Sex
- Female
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
Stress urinary incontinence (SUI) is most prevalent among women. SUI is characterized by loss of urine from increased abdominal pressures caused by coughing, laughing, sneezing, running, lifting or walking. SUI cause women to avoid routine physical activities, thus detracting significantly from their quality of life. The purpose of this study is to evaluate the performance of new designs of the TIPI device, a conservative, disposable, treatment for temporary management of SUI.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | TIPI vaginal pessary | TIPI vaginal pessary G3 model, and TIPI SMD's |
Timeline
- Start date
- 2007-09-01
- Primary completion
- 2009-06-01
- Completion
- 2009-06-01
- First posted
- 2013-01-18
- Last updated
- 2015-01-16
- Results posted
- 2015-01-16
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT01770691. Inclusion in this directory is not an endorsement.