🏛️ Verified NIH Protocol • Sourced via U.S. National Library of Medicine (Last Synced: 2025-12-09)

Rectal Indomethacin and Oral Tacrolimus Versus Combination to Prevent Post-ERCP Pancreatitis

🟢 Recruiting Phase 3 💊 Investigational Drug / Biologic Sponsor: Johns Hopkins University

🩺 Protocol Summary

This research is being done to see if using oral tacrolimus before endoscopy, can prevent pancreatitis that may occur after ERCP (a type of gastrointestinal endoscopy).

Primary Research Facility: Johns Hopkins Hospital (Baltimore, Maryland)

📋 Basic Study Criteria & Logistics Checklist

0 of 3 Checked

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Post-ERCP Acute Pancreatitis?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged 18 Years or older?

🔍 Protocol Specified Minimum Age: 18 Years

Able to attend required in-person clinic visits and study procedures at one of the participating study centers?

🔍 Logistical Requirement: 5 Registered Participating Sites

📍 Primary Site Map

Site: Johns Hopkins Hospital — Baltimore, Maryland

📍 All Participating Trial Locations (5 Sites)

Multi-Center Trial

This protocol is enrolling participants across multiple clinical centers:

1. Johns Hopkins Hospital — Baltimore, Maryland • Contact: (410) 624-6955

2. Asian Institute of Gastroenterology — Hyderabad, Andhra Pradesh

3. Apollo Multispecialty Hospitals, — Kolkata, West Bengal

4. Post Graduate Institute of Medical Education and Research — United States

5. Singapore General Hospital — United States

📄 Print Doctor Discussion Sheet

Preview and print a 1-page summary with 5 tailored questions for your physician.

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.

🏛️ Official Government Provenance

NIH ClinicalTrials.gov Protocol Record

NCT Identifier: NCT05252754 • Last Synced: 2025-12-09

View on ClinicalTrials.gov ↗