EUS- and US- Guided Biopsy for Pancreatic Lesion
Comparison of Safety and Effectiveness Between Endoscopic Ultrasound-guided and Ultrasound-guided Pancreatic Biopsy in Focal Pancreatic Disease: A Multi-center, Retrospective, Propensity Score Analysis
1 other identifier
observational
2,517
0 countries
N/A
Brief Summary
Endoscopic ultrasound (EUS) and ultrasound (US) are the two primary imaging modalities used to guide pancreatic needle biopsy. This study aimed to compare the diagnostic performance and complications associated with EUS- and US-guided pancreatic biopsies.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2025
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 17, 2025
CompletedStudy Start
First participant enrolled
August 18, 2025
CompletedFirst Posted
Study publicly available on registry
August 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedAugust 24, 2025
August 1, 2025
5 months
August 17, 2025
August 17, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
diagnostic inaccuracy
1-year
Interventions
EUS- and US- guided pancreatic biopsy
Eligibility Criteria
consecutive patients with focal pancreatic disease underwent procedures for pancreatic tissue acquisition
You may qualify if:
- Between January 2017 and December 2023, 2663 consecutive patients with focal pancreatic disease underwent 2729 procedures for pancreatic tissue acquisition from focal pancreatic lesions at seven university teaching hospitals in China.
You may not qualify if:
- Patients were excluded from the study if they had less than 12 months of follow-up, were lost to follow-up, had incomplete follow-up data, or underwent intraoperative biopsy or fluid aspiration.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Tian'an Jianglead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Tian'an Jiang
Study Record Dates
First Submitted
August 17, 2025
First Posted
August 24, 2025
Study Start
August 18, 2025
Primary Completion
December 31, 2025
Study Completion
December 31, 2025
Last Updated
August 24, 2025
Record last verified: 2025-08