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

Completed · Not applicable

Conditions studied: Complications; Cesarean Section

In brief

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

Key facts

Study ID

NCT01739543

Run by

Stetrix, Inc.

People needed

102

Starts

2012-04-01

Expected to finish

2013-01-01

Last updated by the study team

2013-03-18

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Subject is scheduled for vaginal delivery.
• Subject is willing and able to comply with the study plan as indicated by understanding and signing the Subject Informed Consent Form.
• Subjects' pre-natal examination indicates that this is to be a single birth delivery.

You may not qualify if…

• Subject's scheduled for vaginal delivery with anticipated complications.
• Subject is unable to understand and sign the informed consent form.
• Subject does not deliver at study facility (hospital).

Where it is running

• Niagara Falls Memorial Medical Center — Niagara Falls, New York, United States

Full record on ClinicalTrials.gov

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