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Comparing Dye-Assisted and Standard Laparoscopic Gallbladder Surgery in Difficult Cases to Reduce Conversion to Open Surgery

Evaluation of the rate of conversion of difficult laparoscopic cholecystectomy as per G10 score by using ICG in comparison to conventional laparoscopic cholecystectomy- A prospective randomized control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100825
Enrollment
100
Registered
2026-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere

Interventions

Intervention1: ICG- guided laparoscopic cholecystectomy: The intervention is ICG-guided laparoscopic cholecystectomy, where patients receive an Intravenous dose of indocyanine green before or during s

Sponsors

Uttar Pradesh institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)All Patients diagnosed with difficult laparoscopic cholecystectomy based on G10 scoring with score 3 or more than 3 2)Willingness to participate in the study.

Exclusion criteria

Exclusion criteria: 1) Patients with contraindications for ICG use. 2) Patients with a history of adverse reactions to ICG. 3) Unstable patients or those with significant comorbidities. 4)History of previous surgery related to HBP or Open Abdominal Surgery.

Design outcomes

Primary

MeasureTime frame
1)Conversion rate to open surgery 2)Success rate of completing laparoscopic cholecystectomy in difficult cases (as per G10 score)Timepoint: Intraoperative (during Calot s triangle dissection).25 minutes—

Secondary

MeasureTime frame
1)Operative time 2)Postoperative complication rates 3)Predictors of success within G10 scoreTimepoint: 1)measured intra-operatively and recorded at case end. 2)ssessed immediate (0 24 h), at discharge, and at 30 days; report severity and related interventions. 3)nalyzed using baseline/pre-operative data (demographics, G10 components) with outcomes (conversion/success) after completion of data collection; report in final analysis (primary dataset). Use identical time-points for both arms. Ensure all intra-operative events—

Countries

India

Contacts

Public ContactDr Somendra pal singh

Uttar pradesh University Of Medical Sciences Saifai, Etawah

somendrachauhan@hotmail.com9719101511

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026