CompletedNot Applicable

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

United States102 participantsStarted 2012-04

Plain-language summary

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

Who can participate

Age range18 Years – 45 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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. Exclusion Criteria: * 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).

What they're measuring

Reduce C-section Rate

Timeframe: 24 hours

Trial details

NCT IDNCT01739543

SponsorStetrix, Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2013-01

View on ClinicalTrials.gov More Complications; Cesarean Section trials