The Effects of Wound Protector to Decrease the Surgical Site Infection in Open Abdominal Surgery, Double-Blind Prospective Randomized Controlled Trial

Phase 3

Completed

• Conditions: Focus on the patient who undergone laparotomy.; Intra- abdominal operation; Laparotomy; Surgical site infection; Wound protector; Wound retractor

• Registration Number: TCTR20180508002
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2018-01-02
• Study Start: 2018-05-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 128

Inclusion Criteria

The patient who have indications for laparotomy surgery
Age between 18-80 years

Exclusion Criteria

The patients who need re-operation
Immunocompromised patients
The patients recieving chemotherapy
The patients recieving abdominal radiation
Pregnancy
The ASA classification more than 3
The patients who did not close the skin as primary closure.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Surgical site infection Everyday in hospital and 30 days after surgery CDC criteria for diagnosis of surgical site infection

Secondary Outcome Measures

Name	Time	Method
/A N/A N/A