ICG dye study for gall bladder laparoscopic surgery
Phase 4
- Conditions
- Health Condition 1: K802- Calculus of gallbladder without cholecystitis
- Registration Number
- CTRI/2023/04/051701
- Lead Sponsor
- DR SANTOSH THORAT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing elective laparoscopic surgery.
Patients of adult age of either sex.
Patients who are willing to participate with informed consent.
Exclusion Criteria
Patients with morbid obesity.
Patients allergic to ICG dye.
Patients hemodynamically unstable for surgery.
Patient not willing to participate in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method intra-operative BILE LEAKTimepoint: day of surgery day zero <br/ ><br>post operative follow up at 3 weeks <br/ ><br>then follow up at 6 months
- Secondary Outcome Measures
Name Time Method delayed Bile leak detection <br/ ><br>anatomical variations seen due to ICG dye useTimepoint: SEEN AT 60 MINUTES POST ICG DYE INJECTION DURING SURGERY