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To compare different methods of doing laparoscopic cholecystectomy i.e. with four holes or single hole

A prospective randomized control trial comparing the outcome of the two modalities of treatment of gall stone disease viz. single incision laparoscopic cholecystectomy with standard 4 port laparoscopic cholecystectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/11/003126
Enrollment
100
Registered
2012-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- ASA 1/2 pateints with gall stone disease

Interventions

Intervention1: Laparoscopic Cholecystectomy using either single port or standard 4 ports: Patients will be randomized into two groups Group 1- Standard Four Port Laparoscopic Cholecystectomy Group

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consecutive patients with gall stone disease

Exclusion criteria

Exclusion criteria: 1.Patients who do not give consent for participation in the study. 2.Patients with morbid obesity. 3.Patients unfit for GA. 4.Patient with uncorrectable coagualopathy 5.Patient with significant co-morbidities like coronary artery disease, asthma, COPD, DM and previous malignancy. 6.Patients requiring other concomitant procedures. 7.Chronic analgesic use

Design outcomes

Primary

MeasureTime frame
To compare the outcome of two modalities of treatment of gall stone disease i.e. standard four port laparoscopic cholecystectomy and single incision laparoscopic cholecystectomy in terms of success, pain, quality of life and cosmesis.Timepoint: Patients will be assessed 24hrs after surgery or at time of discharge whichever is earlier. Follow up at 1 week , 6 weeks, 3months, 6 months and 12 months—

Secondary

MeasureTime frame
Complications, post operative hospital stay and cost effectivenessTimepoint: Postoperative one week to 1 month—

Countries

India

Contacts

Public ContactSidharth Gupta

All India Institute of Medical Sciences, New Delhi, India

mcmisra@gmail.com01126594776

Outcome results

None listed

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