Trials / Completed
CompletedNCT01739543
A Reduction in C-section Rates Using the Hem-Avert Perianal Stabilizer
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 102 (actual)
- Sponsor
- Stetrix, Inc. · Industry
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
A REDUCTION IN C-SECTION RATES USING THE HEM-AVERT® PERIANAL STABILIZER.
Detailed description
This study is being conducted to evaluate an existing FDA approved device called the HEM-AVERT® Perianal Stabilizer for its efficacy in reducing Cesarean births and/or reducing the second stage of labor.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Hem-Avert | Application of Hem-Avert |
Timeline
- Start date
- 2012-04-01
- Primary completion
- 2013-01-01
- Completion
- 2013-01-01
- First posted
- 2012-12-03
- Last updated
- 2013-03-18
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01739543. Inclusion in this directory is not an endorsement.