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Use of Antiseptic Solution for Vaginal Wash Before Cesarean Section

NCT03442218 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 203

Last updated 2019-12-09

No results posted yet for this study

Summary

To evaluate the rate of infections after cesarean sections in patients with premature rupture of membranes after vaginal wash either with an antiseptic solution (clorhexidine solution) vs. saline solution (placebo).

Conditions

  • Operation Wound; Infection
  • Endometritis

Interventions

DRUG

Clorhexidine

Vaginal wash with clorhexidine solution previous to cesarean section in patients with premature rupture of membranes.

DRUG

Saline solution

Vaginal wash with saline solution previous to cesarean section in patients with premature rupture of membranes.

Sponsors & Collaborators

  • Sistema Nacional de Investigación (SNI) - Panamá

    collaborator UNKNOWN

  • Saint Thomas Hospital, Panama

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-01
Primary Completion
2017-08-31
Completion
2018-02-28

Countries

  • Panama

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 NCT03442218 on ClinicalTrials.gov