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Not Yet RecruitingNCT06840041

Vaginal Microbiota and Post-cesarean SSI

The Relationship Between Vaginal Microbiota and Post-Cesarean Section Wound Infection

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
160 (estimated)
Sponsor
Al-Azhar University · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The goal of this observational study is to investigate the relationship between vaginal microbiota composition and the development of post-cesarean section wound infection in women undergoing cesarean delivery. The main question it aims to answer is: Is there a correlation between specific vaginal microbiota profiles and the incidence of post-cesarean section wound infection? Can specific bacterial taxa or diversity indices within the vaginal microbiota predict the risk of post-cesarean section wound infection? Participants will: Provide vaginal swab samples pre-operatively and post-operatively. Undergo standard post-cesarean section care and follow-up. Have wound assessment performed per standard of care, and have data collected regarding wound infection status. Have demographic and clinical data collected, including but not limited to, antibiotic use, gestational age, and comorbidities.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTVaginal swab and cultureParticipants will undergo vaginal swab collection both pre-operatively, immediately prior to the cesarean section, and post-operatively, within a defined timeframe after the procedure. The swabs will be collected using sterile swabs, following standardized procedures to ensure accurate sampling of the vaginal microbiota. The collected samples will then be sent to a designated laboratory for culture and analysis. This process will identify and characterize the bacterial composition of the vaginal microbiota, allowing researchers to investigate potential correlations between specific microbial profiles and the development of post-cesarean section wound infections

Timeline

Start date
2025-06-30
Primary completion
2026-06-30
Completion
2026-07-30
First posted
2025-02-21
Last updated
2025-06-15

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06840041. Inclusion in this directory is not an endorsement.