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Chlorhexidine Vaginal Preparation for Reduction of Post-cesarean Endometritis and Sepsis

NCT04385680 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 840

Last updated 2022-09-23

No results posted yet for this study

Summary

The study aims to assess the beneficial value of vaginal preparation with chlorhexidine gluconate 0.05% before cesarean delivery of cases in labor in reduction of postoperative endometritis, fever and wound complications compared to no preparation or using saline only.

Conditions

  • Postpartum Endometritis
  • Wound Infection
  • Chlorhexidine Adverse Reaction
  • Postoperative Fever

Interventions

DRUG

Chlorhexidine Gluconate vaginal solution 0.05%

preoperative vaginal preparation

Sponsors & Collaborators

  • Zagazig University

    lead OTHER_GOV

Principal Investigators

  • Ahmed Shafiek · Armed forces hospitals Southern Region KSA

  • Hytham Atia · Armed Forces Hospitals Southern Region

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-05-15
Primary Completion
2022-03-10
Completion
2022-08-30

Countries

  • Saudi Arabia

Study Locations

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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 NCT04385680 on ClinicalTrials.gov