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Clinical Trials/JPRN-UMIN000027668
JPRN-UMIN000027668
Completed
Phase 3

Evaluation of the new 22-gauge EUS guided Biopsy Needle (Acqiure) Comparing to another new 20-gauge FNA needle with forward-cutting bevel (ProCore) in Patients With Autoimmune Pancreatitis : A Prospective Randomized, Controlled Multicenter Study - Comparing the diagnostic yield of EUS-FNA using ProCore and Acquire in patients with AIP (COMPAS study)

Bilio-Pancreatic Stenting study group0 sites110 target enrollmentAugust 1, 2017

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
type 1 autoimmune pancreatitis
Sponsor
Bilio-Pancreatic Stenting study group
Enrollment
110
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 1, 2017
End Date
December 31, 2023
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Bilio-Pancreatic Stenting study group

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Uncorrectable coagulopathy (INR \> 1\.5\). Or uncorrectable thrombocytopenia (platelet \< 50,000\) 2\) Uncooperative patients 3\) Inaccessible lesions to EUS 4\) Patients with ASA criteria 3, 4, or 5 5\) Refusal to consent form

Outcomes

Primary Outcomes

Not specified

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