Comparison of two different Suture Material for Port site (Wound) closure in Laparoscopic Abdominal (Belly) Surgeries.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063533
- Lead Sponsor
- DrJuan Jacob
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patient Undergoing Elective Gastro-Intestinal Laparoscopic Surgeries Who Give Consent Are Included In The Study
Exclusion Criteria
Patients Undergoing Emergency Procedures
Patients That Are Immunocompromised
Pregnancy
Patients With Umbilical Hernias
Patients With Previous Laparotomies
Hiv Positive Patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the post Operative port site complication such as port site pain after closure of 10mm umbilical port sitesTimepoint: Patients in both the groups will be assessed on Post Operative day - 1,3,14 using Visual Analogue Scale
- Secondary Outcome Measures
Name Time Method To compare the post Operative port site complication such as surgical site infection after closure of 10mm umbilical port sitesTimepoint: Patients in both the groups will be assessed on Post Operative day - 1,3,14 using Southampton Wound Scoring System