MedTrace Logo

Abnormal Vaginal Flora and Vaginal Lesions at Delivery: is There a Relationship?

NCT01822782 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1100

Last updated 2025-11-19

No results posted yet for this study

Summary

The main objective of this study is to assess whether the presence of abnormal vaginal flora (intermediate flora or vaginosis) is a risk factor for vaginal lesions at the time of delivery. For this, the primary endpoint will be the proportion of vaginal lesions according to the presence or absence of abnormal vaginal flora.

A more precise qualitative and quantitative study of vaginal flora isolated from pregnant women and its association with vaginal lesions will also be conducted.

Conditions

  • Vaginal Lesion

Interventions

BIOLOGICAL

Bacteriological analysis of vaginal sample

Bacteriological analysis of vaginal sample

Sponsors & Collaborators

  • Centre Hospitalier Universitaire de Nīmes

    lead OTHER

Principal Investigators

  • Laurie Becerra, Sage Femme · Centre Hospitalier Universitaire de Nîmes

  • Jean-Philippe Lavigne, MD, PhD · Centre Hospitalier Universitaire de Nîmes

Eligibility

Min Age
15 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-06-30
Primary Completion
2013-12-06
Completion
2013-12-06

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01822782 on ClinicalTrials.gov