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RECRUITING Not applicable ClinicalTrials.gov

Improvised Endobag vs Direct Gallbladder Extraction in Laparoscopic Cholecystectomy

Sponsor: Rawal Institute of Health Sciences Islamabad • ClinicalTrials.gov ID: NCT07823803

Registry updated: 2026-09-16
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Description

Eligigble patients will be enrolled after obtaining informed consent. Basic information such as age, gender, body weight, smoking and alcohol history, number of gallstones, and gallbladder characteristics will be recorded. During surgery, the method used to remove the gallbladder, the port used for extraction, and the duration of surgery will be documented. Any gallbladder perforation, leakage of bile, or spillage of gallstones during the procedure will also be recorded. After surgery, patients will be monitored in the hospital for 24 hours. Their pain will be assessed before discharge. Patients will then be followed in the outpatient clinic for 10 days to assess wound healing and identify any wound infection or other complications. The study aims to compare the safety and effectiveness of an improvised retrieval bag with removal of the gallbladder without a retrieval bag during laparoscopic surgery.

Interventions

  • Endobag (Device)
    Gallbladder will be removed using Endobag
  • placebo group (Device)
    Gallbladder will be removed without using Endobag during Laparoscopic Cholecystectomy

Eligibility criteria

Inclusion Criteria: * Elective Laparoscopic Cholecystectomy Exclusion Criteria: * Patients having common bile duct stones or dilatation * Acute cholecystitis, gallbladder perforation, malignancy (on medical record). * Patients requiring conversion to open cholecystectomy, ASA III-IV * Patients with skin diseases near wound site, diabetes (HbA1c\>6.5%), and Hb \<10gm/dl

Conditions

Cholecystectomy, Laparoscopic Cholelithiasis

Locations

  • Rawal Institute of Health Sciences — Islamabad, Federal, Pakistan
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record