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NCT05678218Completed

Preoperative Evaluation of Lymph Nodes of Cholangiocarcinoma

Preoperative Evaluation of Lymph Nodes of Cholangiocarcinoma - a Registration Study

Source: ClinicalTrials.gov · Last updated 8 Aug 2025

Brief summary (registry, in English)

The goal of this observational cohort study is to assess the yield of preoperative endoscopic ultrasound focussed on lymph nodes in patients with presumed resectable perihilar (pCCA), intrahepatic (iCCA) or mid-common bile duct (CBD) cholangiocarcinoma. The main questions it aims to answer is: 1. The number of patients precluded from surgical work-up due to positive regional or extraregional lymph nodes identified by endoscopic ultrasound guided tissue acquisition 2. Characteristics during endoscopic ultrasound of lymph nodes associated with malignancy

Status (registry)
Completed
Study type
Observational
Enrollment
245 (actual)
First submitted
23 Dec 2022
Start date
5 Sept 2022
Primary completion date
1 Jul 2025
Lead sponsor
Erasmus Medical Center
NCT number
NCT05678218

What you commit to

  • Study type: Observational
  • Participants enrolled: 245
  • From 5 Sept 2022 to the primary completion date, 1 Jul 2025
  • 7 sites in 2 countries
  • 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 illness

  • Patients with a history of treated CCA
  • Patients with a history of treated liver malignancy

Lab values

  • Patients with a contra-indication for EUS-tissue acquisition (f.e. uncorrectable coagulopathy or platelet disorder), in line with current clinical practice

Other

  • Patients with CCA for which a pancreatoduodenectomy is indicated, based on cross-sectional imaging

Who the study is looking for

  • Presumed resectable pCCA OR
  • Presumed resectable iCCA OR
  • Presumed resectable mid-common bile duct CCA OR
  • Presumed unresectable pCCA worked-up for Liver Transplantation AND
  • Written informed consent must be given according to International Council on Harmonisation/Good Clinical Practice guidelines, and national/local regulations AND
  • Age \> 18 years.

Age in the registry: 18 years to 110 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

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

SiteCityCountrySite status
University Hospital of Ghent
Coordinator of this site? Confirm its status
GhentBelgiumUnknown status
Amsterdam University Medical Center
Coordinator of this site? Confirm its status
AmsterdamNetherlandsUnknown status
University Medical Center Groningen
Coordinator of this site? Confirm its status
GroningenNetherlandsUnknown status
Leiden University Medical Center
Coordinator of this site? Confirm its status
LeidenNetherlandsUnknown status
Maastricht UMC
Coordinator of this site? Confirm its status
MaastrichtNetherlandsUnknown status
Erasmus University Medical Center
Coordinator of this site? Confirm its status
RotterdamNetherlandsUnknown status
University Medical Center Utrecht
Coordinator of this site? Confirm its status
UtrechtNetherlandsUnknown status

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