A Reduction in C-section Rates Using the Hem-Avert Perianal Stabilizer

Status Completed

Clinical Trial Summary

A REDUCTION IN C-SECTION RATES USING THE HEM-AVERT® PERIANAL STABILIZER.

Clinical Trial 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. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Complications; Cesarean Section

Clinical Trial Details

NCT number	NCT01739543
Study type	Interventional
Source	Plexus Biomedical, Inc.
Contact
Status	Completed
Phase	N/A
Start date	April 2012
Completion date	January 2013

View Details

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