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Impact of fluorescent imaging on operating time of laparoscopic gall bladder surgery.

Comparison of operating time in Laparoscopic Cholecystectomy with or without Near Infrared Fluorescence Cholangiography: A Randomised Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052934
Enrollment
70
Registered
2023-05-19
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: K801- Calculus of gallbladder with othercholecystitis Health Condition 2: K819- Cholecystitis, unspecified

Interventions

Intervention1: Indocyanine green (ICG) assisted near-infrared fluorescence cholangiography (NIRF) during laparoscopic cholecystectomy (LC): Laparoscopic NIRF imaging equipment will be used to perform

Sponsors

All India Institute of Medical Sciences, Jodhpur
Lead Sponsor
Aishwarya
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Consenting adults undergoing elective laparoscopic cholecystectomy

Exclusion criteria

Exclusion criteria: 1. Sensitive to ICG or iodine 2. Hepatic or renal insufficiency 3. Pregnant or lactating female 4. Preoperative diagnosed malignancy or suspicion of GB malignancy 5. Emergency cholecystectomy 6. Cholecystectomy performed as part of another procedure (such as CBD exploration, choledochal cyst excision, whippleâ??s operation) or incidental cholecystectomy done concomitantly with another procedure

Design outcomes

Primary

MeasureTime frame
To compare the operating time in patients undergoing conventional elective LC versus NIRF assisted LCTimepoint: Intraoperatively

Secondary

MeasureTime frame
To compare frequency of CVS achievementTimepoint: Intraoperatively;To compare frequency of intra-operative bile leak or biliary duct injuryTimepoint: Intraoperatively;To compare the frequency of detection of biliary tree anomalies pre-dissectionTimepoint: Intraoperatively;To compare the operative difficulty in two groups (Nassar grading)Timepoint: Intraoperatively;To compare time to demonstration of CVSTimepoint: Intraoperatively;To compare Clavien-Dindo grades of complicationsTimepoint: Day 1, Day 7 and on Day 30 postoperatively;To compare frequency of conversion to open surgeryTimepoint: Intraoperatively

Countries

India

Contacts

Public ContactDr Mahaveer Singh Rodha

AIIMS Jodhpur

msrodha@gmail.com8003996885

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026