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NCT06416397Recruiting

Diagnostic Approach for Cholangiocarcinoma Using Liquid Bile Biopsy

Source: ClinicalTrials.gov · Last updated 16 Dec 2025

Brief summary (registry, in English)

The main aim of the study is to develop a diagnostic proteomic profile of cholangiocarcinoma using bile samples. The primary endpoint will be the rate of concordant positive diagnoses obtained from bile samples based on proteomic profiling compared with histological reference diagnoses (concomitant cytological sampling and/or final histological sampling).

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
1 Feb 2024
Start date
8 Apr 2025
Primary completion date
Feb 2026
Lead sponsor
University Hospital, Bordeaux
NCT number
NCT06416397

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 8 Apr 2025 to the primary completion date, Feb 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Pregnant woman
  • Patient under legal protection

Who the study is looking for

  • Patient 18 years and older
  • Patients with bile duct stenosis who require endoscopy with retrograde papillary catheterization or a radiological procedure for diagnostic purposes (histological samples) as part of their management
  • Oral consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Bordeaux
Coordinator of this site? Confirm its status
PessacFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.