Terminated PHASE3 INTERVENTIONAL 2-arm NCT00528008

A Comparison of Surgical Preparations and Wound Infection Rates for Elective Cesarean Sections

Povidone-iodine vs. Chlorhexidine Gluconate - A Comparison of Surgical Preparations and Wound Infection Rates for Elective Cesarean Sections

Sponsor: Eastern Health

Conditions Wound Infection

Interventions chlorhexidine gluconate povidone-iodine solution

Updated 5 times since 2017 Last updated: Nov 8, 2012 Started: Dec 31, 2007 Primary completion: Feb 28, 2010 Completion: Feb 28, 2010

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Study was stopped following interim analysis.

Other terminated trials from Eastern Health

Corona Virus Infection · Phase PHASE3 · Aug 2020

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Other Wound Infection trials with similar outcome

NCT01169064 · Phase NA · Jul 2012

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Listed as NCT00528008, this PHASE3 trial focuses on Wound Infection and remains terminated or withdrawn. Sponsored by Eastern Health, it has been updated 5 times since 2007, reflecting limited change activity. This study is part of the global effort to build evidence for infectious disease interventions.

Status Flow

Change History

5 versions recorded

Sep 2024 — Present [monthly]

Terminated PHASE3
Jul 2024 — Sep 2024 [monthly]

Terminated PHASE3
Jan 2021 — Jul 2024 [monthly]

Terminated PHASE3
Jun 2018 — Jan 2021 [monthly]

Terminated PHASE3
Jan 2017 — Jun 2018 [monthly]

Terminated PHASE3

First recorded

Dec 2007

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Eastern Health
Memorial University of Newfoundland

Data source: Memorial University of Newfoundland

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• St. John's, Canada