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Perineal Echography in the Delivery Room for the Detection of Anal Lesions — OASIS 1  

Parturition Clinical Trial

Official title:
Perineal Echography in the Delivery Room for the Detection of Anal Lesions Among Primiparous Mothers: a Randomized Study

Clinical Trial Summary

The main objective of this study is to compare the rate of anal incontinence (measured by the Wexner score, qualitative and quantitative (> 4)) at 3 months post partum among primiparas with vaginal tears ≥ 2nd degree who receive a sphincter injury screening at delivery by conducting a sphincter ultrasound in the delivery room versus a similar group of women who do not benefit from screening.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01320995
Study type Interventional
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Terminated
Phase N/A
Start date September 2011
Completion date March 2014
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