ClinicalTrials.Veeva

Menu

Does Subtotal Cholecystectomy Rate for Acute Cholecystitis Change With a Previous ERCP?

B

Bakirkoy Dr. Sadi Konuk Training and Research Hospital

Status

Completed

Conditions

Cholangiopancreatography, Endoscopic Retrograde
Cholecystectomy, Laparoscopic

Treatments

Procedure: ERCP

Study type

Observational

Funder types

Other

Identifiers

NCT05728073
20230205

Details and patient eligibility

About

Study is designed to investigate whether the history of ERCP is associated with subtotal cholecystectomy rates in patients underwent laparoscopic cholecystectomy operations with the diagnosis of acute cholecystitis.

Full description

The results of patients who underwent surgery for acute cholecystitis in a single center between January 2016 and December 2019 were included and evaluated retrospectively.

Primary outcome was subtotal cholecystectomy rate. Secondary outcomes were conversion to open, complications and serious complications. Within examining demographic findings, operative records (rates for subtotal cholecystectomy and conversion to open, operative duration) and follow-up results (postoperative complications, serious complications, length of hospital stay and mortality) for all cases were investigated. Complications that Clavien-Dindo Score ≥ 3 accepted as serious complication. Intraoperative detection of gallbladder perforation was also noted and included in comparison. Any biliary tract complication that needed any percutaneous or endoscopic intervention to handle was named as "biliary leak" in the study.

Enrollment

470 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients operated with the diagnosis of acute cholecystitis with an age greater or equal to 18 years old in a single center between January 2016 and December 2019

Exclusion criteria

  • Initial and direct preferance of open method
  • Being diagnosed with malignity after histopathological evaluation
  • Being operated just before one week after ERCP or after more than six weeks after ERCP

Trial design

470 participants in 2 patient groups

Standard (non-ERCP) Group
Description:
Patients who underwent surgery for acute cholecystitis without a previous ERCP history.
ERCP group
Description:
Patients who underwent surgery for acute cholecystitis with a previous ERCP history.
Treatment:
Procedure: ERCP

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems