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The Effect of Timing of Removal of Wound Dressing on Surgical Site Infection Rate After Cesarean Delivery

NCT02902419 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 602

Last updated 2016-09-15

No results posted yet for this study

Summary

A randomized controlled trial measuring surgical site infection rate as a function of timing of wound dressing removal.

Conditions

  • Surgical Site Infection

Interventions

OTHER

Wound dressing removal.

Sponsors & Collaborators

  • Albany Medical College

    lead OTHER

Principal Investigators

  • Peter R Cole, MD · Albany Medical College

  • Kevin C Kiley, MD · Albany Medical College

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2012-03-31
Completion
2012-05-31

Countries

  • United States

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 NCT02902419 on ClinicalTrials.gov