Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06978231

Effect of Same-session EUS on ERCP in Pancreaticobiliary Diseases

Led by Qilu Hospital of Shandong University · Updated on 2025-09-09

214

Participants Needed

1

Research Sites

94 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is a single-center randomized controlled trial. Eligible subjects meeting inclusion/exclusion criteria will be randomized 1:1 to EUS+ERCP group or ERCP group. Clinical data and patient-reported outcomes are regularly collected at baseline and during follow-up periods. A comparative analysis was conducted to assess the impact of same-session EUS on ERCP strategy modification between two groups, utilizing a structured questionnaire.Secondarily, the safety and efficacy of same-session EUS will be comprehensively evaluated by comparing complication rates, technical success rate and hospitalization costs, length of stay, and radiation exposure between groups.

CONDITIONS

Official Title

Effect of Same-session EUS on ERCP in Pancreaticobiliary Diseases

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years
  • Patients with pancreaticobiliary diseases definitively indicated for ERCP as confirmed by hepatobiliary-pancreatic specialists
  • No prior history of ERCP
  • No pancreaticobiliary EUS examinations within the preceding 3 months
Not Eligible

You will not qualify if you...

  • Patients with malignant lesions deemed surgically unresectable requiring pathology only for chemotherapy/radiotherapy guidance
  • Patients requiring only palliative biliary or pancreatic stent placement for obstructive jaundice
  • Patients with anatomical changes or surgical history preventing EUS feasibility
  • Severe systemic illnesses including serious liver, kidney, heart, lung, or brain diseases that increase risk for endoscopy
  • Contraindications to iodinated contrast media such as allergy or renal impairment
  • Pregnancy or breastfeeding
  • Severe bleeding disorders
  • Declined informed consent
  • Severe psychiatric disorders or inability to cooperate making safe procedure impossible

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Qilu Hospital of Shandong University

Jinan, Shandong, China, 250000

Actively Recruiting

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Research Team

Z

Zhen Li, MD,PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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