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NCT05021315

Vaginal Cleaning Using Povidone Iodine Before CS to Reduce Postoperative Wound Infection

Status unknown Phase 3 Last updated 18 July 2022
What this trial tests

Phase 3 trial testing 10% povidone iodine in Cesarean Section Complications in 800 participants. Status unknown.

Timeline
15 September 2021
Primary endpoint
30 September 2022
15 October 2022

Quick facts

Lead sponsorCairo University
PhasePhase 3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment800
Start date15 September 2021
Primary completion30 September 2022
Estimated completion15 October 2022
Sites2 locations across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 18 to 38, female only, with Cesarean Section Complications or Vaginal Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of work to assess the effectiveness of preoperative vaginal cleansing with povidone iodine on reduction of post caesarean section wound infection Research questions: Does vaginal cleaning using povidone iodine before cesarean section has effect on reduction of postoperative wound infection??

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of 10% povidone iodine

Trials testing the same drug.

Other recruiting trials for Cesarean Section Complications

Currently open trials in the same condition.

Other Cairo University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05021315.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing