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Sterile vs Clean Non-Sterile Wound Dressing in Orthopedic Surgery

NCT07436065 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2026-02-27

No results posted yet for this study

Summary

This randomized interventional pilot study aims to compare the rate of significant Surgical Site Infection (SSI) within the six weeks after elective orthopedic surgery using sterile versus clean non-sterile glove postoperative dressing techniques.

Conditions

  • Surgical Site Infection (SSI)

Interventions

PROCEDURE

Sterile Glove Dressing Technique

Postoperative wound dressing performed using sterile glove with standard aseptic technique

PROCEDURE

Clean Non-Sterile Glove Dressing Technique

Postoperative wound dressing performed using clean non-sterile glove with standard aseptic technique

Sponsors & Collaborators

  • Hamad Medical Corporation

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-01
Primary Completion
2022-12-14
Completion
2024-12-14

Countries

  • Qatar

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 NCT07436065 on ClinicalTrials.gov