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Clinical Trials/PACTR201709002597110
PACTR201709002597110
Not yet recruiting
未知

Effectiveness of Preoperative Vaginal Cleansing with Povidone-Iodine in Post-ceasarean Infectious Morbidity; A Randomized Controlled Trial.

The authors0 sites180 target enrollmentSeptember 8, 2017
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ConditionsPregnancy and ChildbirthSurgeryPost-operative caesarean infectious morbidity

Overview

Phase
未知
Intervention
Not specified
Conditions
Pregnancy and Childbirth
Sponsor
The authors
Enrollment
180
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 8, 2017
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
The authors

Eligibility Criteria

Inclusion Criteria

  • •All consenting parturients admitted in FETHA for either elective or emergency caesarean section after 37 completed weeks.

Exclusion Criteria

  • •Refusal of consent.
  • •Women with known allergy to topical povidone\-iodine
  • •Placenta praevia.
  • •Cord prolapse
  • •Clinical Chorioamnionitis
  • •Foul smelling discharge on admission.
  • •Women with immunosupression due to HIV/AIDS, Diabetes Miletus or chronic use of steroids.

Outcomes

Primary Outcomes

Not specified

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