← Eichor
Study identifier: NCT06978231 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Same-session EUS on ERCP in Pancreaticobiliary Diseases

Condition: Pancreaticobiilary Diseases  ·  Sponsor: Qilu Hospital of Shandong University

PhaseNA
Planned participants214
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Zhen Li, MD,PhD  ·  +86 18560086106  ·  qilulizhen@sdu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Qilu Hospital of Shandong UniversityJinan, Shandong, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06978231