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ClustEr randomisEd Trial of sterile glove And instrument change at the time of wound closure to reduce surgical site infection in Low and Middle Income Countries (LMICs)

Phase 4
Conditions
Surgery
Registration Number
PACTR202008463834676
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
12800
Inclusion Criteria

Hospital Inclusion Criteria
1. Hospitals where glove and instrument change is not currently routine practice.
Patient Inclusion Criteria
Patients undergoing abdominal surgery who satisfy the following criteria are eligible:
1a. Emergency (surgery on an unplanned admission) or elective (surgery on a planned admission)
1b. Intraoperative finding of clean-contaminated, contaminated or dirty surgery.
1c. With at least one abdominal incision that is =5cm

Exclusion Criteria

Patients undergoing caesarean section.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Surgical Site Infection
Secondary Outcome Measures
NameTimeMethod
1.SSI before discharge from hospital.<br>2.Unexpected re-admission into hospital for a wound-related problem within 30-days post surgery.<br>3.Unexpected re-operation for a wound-related problem within 30-days post surgery.<br>4.Length of hospital stay.<br>5.Return to normal activities (e.g. work, school, or family duties) within 30-days post surgery.<br>6.Death within 30 days of surgery<br>
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