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Clinical Trials in Canada / NCT05141916
Recruiting Observational

Optimizing the Evaluation and Management of Patients With Suspected Choledocholithiasis

NCT05141916 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2019-02-25
Last updated
2026-04-29

Condition(s) studied

Biliary DiseaseCholedocholithiasis

Investigational drug(s) / intervention(s)

Endoscopic Retrograde Cholagiopancreatography (ERCP)

Endoscopic Retrograde Cholagiopancreatography (ERCP): Endoscopic procedure employed to manage biliary and pancreatic diseases

Study summary

Choledocholithiasis (stone(s) in the common bile duct) is common. Untreated or missed, choledocholithiasis has high morbidity and mortality. Endoscopic retrograde cholangio-pancreatography (ERCP) is recognized as the first-line modality for management. While effective, ERCP is associated with adverse events. Thus, the selection of patients for ERCP should be accompanied by a high pre-test suspicion of choledocholithiasis.

Choledocholithiasis is suspected based on clinical, biochemical and radiographic findings. The most relied-upon strategy for risk stratification of choledocholithiasis is based on guidelines from The American Society for Gastrointestinal Endoscopy (ASGE). In it, clinical predictors are defined as "very strong", "strong" or "moderate", and the presence of one or more of these is meant to suggest "high" or "intermediate" probability of choledocholithiasis.

A knowledge gap exists in the performance characteristics of intermediate-probability criteria, where overall accuracy is \<50% from limited data. Patients in this group are recommended to a) undergo endoscopic ultrasound (EUS) or magnetic resonance cholangio-pancreatography (MRCP), b) undergo cholecystectomy with intra-operative cholangiography (IOC), or c) proceed directly to ERCP. At centres where EUS and MRCP are readily available, these are preferred options, as they are least invasive and sensitive; however, they are often unavailable. Thus, in clinical practice, a high proportion of intermediate-risk patients ultimately proceed directly to ERCP, where likelihood of benefit is only moderate, while procedural risk remains.

The role of liver enzyme changes has not been evaluated; however, dynamic changes may offer another method for evaluating patients at intermediate risk of CBD stones that is safe and available. Incorporation of dynamic liver enzymes may improve the test-performance characteristics of the existing framework.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with suspected choledocholithiasis, regardless of probability * age 18 years old or older * able to give informed consent to involvement (in the prospective validation phase). Exclusion Criteria: * Unable or unwilling to provide informed consent; * age \< 18 years; * suspected or proven cholangitis; * previous ERCP with sphincterotomy; * prior diagnosis or management of choledocholithiasis; * outpatient status; * out-of-province status (prohibiting full medical record access).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Calgary Calgary Alberta Recruiting

More University of Calgary trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05141916 on ClinicalTrials.gov ↗ ← All trials in Canada