CTRI/2024/03/063533
Not yet recruiting
Phase 4
Comparison of non absorbable Polypropylene and absorbable Polydioxanone Suture for Umbilical Port site closure - A Randomised Controlled Trial - Nil
DrJuan Jacob0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: O- Medical and Surgical
- Sponsor
- DrJuan Jacob
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
- •Patients With Umbilical Hernias
- •Patients With Previous Laparotomies
- •Hiv Positive Patients
Outcomes
Primary Outcomes
Not specified
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