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Recruiting NCT07130864

Early vs Late Laparoscopic Cholecystectomy After Common Bile Duct Stones Clearance Through Ercp.

No phase Interventional Laparoscopic Cholecystectomy Choledocholithiasis ERCP Bile Duct Injury

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Early cholecystectomy, Late cholecystectomy.
Who it may be relevant to
Registry conditions: Laparoscopic Cholecystectomy, Choledocholithiasis, ERCP, Bile Duct Injury. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Early Vs Late Laparoscopic Cholecystectomy After Ercp For Choledocholithiasis, A Randomised Control Trial.

Overview

There is controversy about timing of cholecystectomy after the common bile duct is cleared of stones. our study aims to compare the results of early vs late cholecystectomy.

Interventions

  • Procedure Early cholecystectomy
    Early cholecystectomy is performed within 72 hours of ERCP.
  • Procedure Late cholecystectomy
    Late cholecystectomy is performed after 72 hours of ERCP

Primary outcome measures

  • Difficulty level of cholecystectomy [Time frame: From start of surgery till end, On day 1 of surgery]
Secondary outcome measures (2)
  • Bile duct injury [Time frame: From the day 1 of surgery till one month]
  • Hospital stay [Time frame: from day 1 of surgery till discharge, upto 1 month]

Eligibility criteria

Inclusion criteria

.All patients undergoing laparoscopic cholecystectomy who had concomitant choledocholithiasis for which ercp is done.

Exclusion criteria

.Non consenting indviduals

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Khyber teaching hospital — Peshawar

Identifiers

NCT: NCT07130864 · 530/DME/KMC

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗