Actively Recruiting

Age: 18Years +
All Genders
NCT07449897

Cholecystectomy With Intraoperative Management of Bile Duct Stones in Norway - the BILNOR Study

Led by Oslo University Hospital · Updated on 2026-03-06

340

Participants Needed

1

Research Sites

565 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The BILNOR study is a prospective multicenter observational study evaluating how common bile duct stones are best managed in patients undergoing cholecystectomy. The study focuses particularly on transcystic laparoscopic common bile duct exploration (LCBDE) and assesses stone clearance, technical success, complications, and health-economic outcomes in routine clinical practice. A secondary aim is to compare LCBDE with intraoperative ERCP regarding efficacy, complication rates, and costs. Approximately 340 patients from several Norwegian centers are planned to be included starting in March 2026.

CONDITIONS

Official Title

Cholecystectomy With Intraoperative Management of Bile Duct Stones in Norway - the BILNOR Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Preoperatively image proven choledocholithiasis or bile duct sludge (US / CT / MRI)
  • Stone size 8 mm or smaller
  • Five or fewer stones
  • Stones not located in the proximal bile duct
  • Planned cholecystectomy with intraoperative bile duct clearance using LCBDE or intraoperative ERCP
Not Eligible

You will not qualify if you...

  • Previous cholecystectomy
  • Medically unfit for surgery due to frailty or other health conditions
  • Technically inoperable due to hostile abdomen, inflammatory processes, bleeding conditions, or cirrhosis
  • Pregnancy

AI-Screening

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Trial Site Locations

Total: 1 location

1

Oslo University Hospital

Oslo, Norway

Actively Recruiting

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Research Team

M

Magnus H Fasting, MD, PhD, FEBS (UGI)

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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