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NCT05865821

Protocol Effect of Negative Pressure Drain to Reducing Surgical Site Infection in Surgical Wound of Abdominal Surgery

Protocol Effect of Negative Pressure Drain to Reducing Surgical Site Infection in Clean-contaminated and Contaminated Surgical Wound of Abdominal Surgery
Mahidol University·ClinicalTrials.gov·procedureEnrolling by invitation
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Study focus
Disease/Condition
Surgical Site Infection
Drug/Device/Intervention
Negative pressure drainage
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
Mahidol University
Location
Bangkok, Thailand
Timeline & enrollment
Phase
N/A
Start date
Apr 15, 2023
End date
Mar 30, 2025
Enrollment
130 participants
Primary outcome

Rate of SSI,Rate of SSI,Rate of SSI,Rate of SSI

Summary

Surgical site infection (SSI) is one of main complication in surgery. It usually occurs
 within 30 days post operation. The superficial SSI is an infection of skin and subcutaneous
 layer, clinically presented by pus oozing. Furthermore, seroma hematoma and wound dehiscence
 are also clinical signs of superficial SSI.
 
 Nowadays, there are studies which report methods reducing SSI by placing negative pressure
 drain within surgical wound. It can reduce serum in subcutaneous layer which is found in
 every surgical wound, especially in clean-contaminated and contaminated wound. Many studies
 show that placing negative pressure drainage within a surgical wound can reduce superficial
 SSI and decrease hospital length of stay by comparing with the control group.
 
 The objective in this study to compare the rate of SSI of clean-contaminated and contaminated
 surgical wounds between the patients whose wounds are placed with negative pressure drainage
 and patients who were not placed with negative pressure drainage.

ICD-10 classifications
Infection following a procedure, not elsewhere classifiedBacterial infection of unspecified siteOther bacterial infections of unspecified siteInfection of obstetric surgical woundOther specified local infections of skin and subcutaneous tissue
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05865821
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05865821 through Pure Global AI's free database. This phase not specified trial is sponsored by Mahidol University and is currently Enrolling by invitation. The study focuses on Surgical Site Infection. Target enrollment is 130 participants.

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