Comparative study of coupling device verses hand-sewn venous anastomosis: a Randomized Controlled Trial
Not Applicable
- Conditions
- Health Condition 1: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx
- Registration Number
- CTRI/2024/08/072517
- Lead Sponsor
- Army Hospital Research and Referral
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Both genders will be selected for the study.
Exclusion Criteria
Recipient vessel size more than 4.0mm or less than 1.0mm.
Patients who have undergone radiation therapy prior to surgery.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Flap conditionTimepoint: Whether the flap has failed or successful will be determined on 5th operative day.
- Secondary Outcome Measures
Name Time Method Rate of flap failures. Return to operation theatre due to venous thrombosis. Surgeon’s fatigue using Samn Perelli scale.Timepoint: Flap monitoring every 2hours for first 24 hours then every 4th hour for next 2nd day and every 6th hour for 3rd, 4th and 5th day. Surgeon’s fatigue will be assessed at end of surgery.