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Bacterial Colonization With and Without Iodophor-impregnated Adhesive Drapes in Hip Surgery: a Prospective, Randomized Trial | Clinical Trials | Clareo Health

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Bacterial Colonization With and Without Iodophor-impregnated Adhesive Drapes in Hip Surgery: a Prospective, Randomized Trial

NCT02919410•Rothman Institute Orthopaedics

View on ClinicalTrials.gov

Summary

This is a prospective, randomized control trial evaluating the efficacy of iodophor-impregnated adhesive drapes for reducing bacterial count in hip surgery.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Primary femoroacetabular osteoplasty (FAO) patients
•Primary Periacetabular Osteotomy (PAO) patients

Exclusion Criteria

•Total hip arthroplasty (THA) patients
•Revision FAO surgery
•Septic or septic arthritis patients
•Patients with systemic or topical allergy to iodine

Key Dates

Start Date

October 1, 2014

Primary Completion Date

May 1, 2016

Last Updated

September 29, 2016

Conditions

Surgical Wound Infection

Interventions

iodophor-impregnated adhesive drapes

DEVICE

No adhesive drapes

OTHER

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Surgical Wound InfectionTraumatic Wound Infection

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: September 29, 2016Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions

Bacterial Colonization With and Without Iodophor-impregnated Adhesive Drapes in Hip Surgery: a Prospective, Randomized Trial

Inclusion Criteria

Exclusion Criteria

A Study of Amicidin-β Topical Solution for Patients With Surgical or Traumatic Wound Infections

Clinical Trial to Demonstrate the Safety and Efficacy of DUOFAG®

To Explore the Effectiveness and Feasibility of HERADERM Hydrogel Wound Dressing on Caesarean Section Surgical Site

Post Cesarian Section Wound Infections At Emergency Room

Antibacterial-coated Sutures at Time of Cesarean

Study the Efficacy of Topical Antibiotherapy in the Prophylaxis of Incisional Surgical Infection in Colorectal Surgery