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Clinical Trials/PACTR202308689414142
PACTR202308689414142
Recruiting
未知

Effect of preoperative vaginal preparation with 0.3% chlorhexidine-cetrimide versus 10% povidone-iodine on post cesarean section infection.

OHIOMOBA GLADYS0 sites250 target enrollmentJuly 21, 2023
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ConditionsSURGICAL SITE INFECTIONS, ENDOMETRITIS AND ENDOMYOMETRITIS

Overview

Phase
未知
Intervention
Not specified
Conditions
SURGICAL SITE INFECTIONS, ENDOMETRITIS AND ENDOMYOMETRITIS
Sponsor
OHIOMOBA GLADYS
Enrollment
250
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 21, 2023
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
OHIOMOBA GLADYS

Eligibility Criteria

Inclusion Criteria

  • •Ages eligible for study: \=18 years
  • •\- All pregnant women with gestational age of 28 weeks and above.
  • •\- Pregnant women with indication for emergency or elective Cesarean section.
  • •\- Patient must give informed consent.

Exclusion Criteria

  • •\-Allergy/Contraindications to either Povidone\-Iodine (thyroid disease) and Chlorhexidine
  • •\-Obstructed Labour
  • •\-Active genital herpes
  • •\-Face Presentation
  • •\-Antepartum hemorrhage, cord prolapse with life fetus
  • •\-Active Chorioamnionitis,
  • •\-Women on chronic steroid use, Diabetes Mellitus, HIV infection,
  • •\-Intrauterine Fetal Death
  • •\-Evidence of pre\-operative skin infection
  • •\-Women considered for a hysterectomy at the time a decision for Cesarean section was made were also excluded.

Outcomes

Primary Outcomes

Not specified

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