Clinical Trials Directory

Trials / Unknown

UnknownNCT05090176

Title: Povidone-soaked Sutures Versus Ordinary Sutures for Reducing Surgical Site Infection

Title: Povidone-soaked Sutures Versus Ordinary Sutures for Reducing Surgical Site Infection: Randomize Control Trial Study in General Surgery Cases of Hospital Universiti Sains Malaysia

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
140 (actual)
Sponsor
Universiti Sains Malaysia · Academic / Other
Sex
All
Age
12 Years
Healthy volunteers
Accepted

Summary

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

Detailed 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

Conditions

Interventions

TypeNameDescription
OTHERpovidone-soaked suturesuture soak with povidone solution for 3 mins
OTHERordinary suturesuture no need to soak with povidone solution

Timeline

Start date
2020-11-02
Primary completion
2021-05-30
Completion
2021-11-02
First posted
2021-10-22
Last updated
2021-10-22

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT05090176. Inclusion in this directory is not an endorsement.