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Endoscopic Ultrasound Evaluation of the Common Bile Duct in Patients With Obstructive Jaundice Due to Bilio-pancreatic Malignancies (ECCO Trial)

Endoscopic Ultrasound Evaluation of the Common Bile Duct in Patients With Obstructive Jaundice Due to Bilio-pancreatic Malignancies: a Multicenter Prospective Study (ECCO Trial)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05155475
Acronym
ECCO
Enrollment
20
Registered
2021-12-13
Start date
2019-06-04
Completion date
2019-12-18
Last updated
2026-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bilio-pancreatic Tumor, Obstructive Jaundice

Brief summary

To assess the size of the common bile duct in a large cohort of patients with jaundice following a malignant tumor of the head of the pancreas or the distal bile duct receiving a diagnostic EA for biopsy and / or for evaluation of tissue resectability.

Interventions

PROCEDUREUltrasound endoscopy

After identification of the lesion, the common bile duct will be identified and followed by the point of dilation due to the compression of the known lesion up to the hilum of the liver

Sponsors

GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead SponsorOTHER
European Clinical Trial Experts Network
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with jaundice and an injury to the head of the pancreas recommended for EUS-guided tissue acquisition or staging * Patients with jaundice and distal CBD lesion suggestive of cholangiocarcinoma or Vater's ampulla carcinoma recommended for EUS-guided tissue acquisition or staging * Serum bilirubin level ≥ 3 mg / dl * Age ≥ 18 years old * Subject affiliated or beneficiary of a social security scheme. * Subject having been informed of this study and having given his no objection

Exclusion criteria

* Presence of altered anatomy due to previous gastric surgery (Billroth II or Roux-en-Y anastomosis) * Sphincterotomy performed previously, plastic biliary stent or metal stent placement * Percutaneous drainage of the bile ducts performed previously * Pregnant, breastfeeding or parturient woman * Protected patients: Adults under guardianship, curatorship or other legal protection, deprived of their liberty by judicial or administrative decision; hospitalized without consent.

Design outcomes

Primary

MeasureTime frame
Evaluation of the common bile duct size1 day

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026