Clinical Trials Directory

Trials / Completed

CompletedNCT01822782

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

Status
Completed
Phase
Study type
Observational
Enrollment
1,100 (actual)
Sponsor
Centre Hospitalier Universitaire de Nīmes · Academic / Other
Sex
Female
Age
15 Years – 45 Years
Healthy volunteers
Not accepted

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

Interventions

TypeNameDescription
BIOLOGICALBacteriological analysis of vaginal sampleBacteriological analysis of vaginal sample

Timeline

Start date
2013-06-01
Primary completion
2013-12-06
Completion
2013-12-06
First posted
2013-04-02
Last updated
2025-11-19

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01822782. Inclusion in this directory is not an endorsement.