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Clinical Trial Summary

To determine efficacy of using 3 minutes povidone-soaked suture in reducing surgical site infection during wound closure in elective surgery.


Clinical Trial Description

Participant recruitment and randomisation based on eligibility based on CONSORT. Patient will get either package A or B which determine whether they are getting povidone-soaked suture or ordinary suture during wound closure. Postoperative, follow up on D10 and D30 of patient well being and signs and symptoms of surgical site infection ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05090176
Study type Interventional
Source Universiti Sains Malaysia
Contact
Status Active, not recruiting
Phase N/A
Start date November 2, 2020
Completion date November 2, 2021