๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-04-28

Short-term Intravenous Fluids for Prevention of Post-ERCP Pancreatitis (NCT06260878)

๐ŸŸข Recruiting Phase4 ๐Ÿ“‹ Clinical Research Protocol Sponsor: University of Calgary

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This study will explore the efficacies of several practical short-term (peri-procedural) intravenous fluid regimens in the prevention of post- endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis (PEP). PEP is the most common serious ERCP-related adverse event (AE), occurring in 5-15% of patients, and associated with significant morbidity, mortality, and healthcare utilization. Given the current lack of data on effectiveness of short-term fluid regimens in PEP prevention to inform practice, the results of the proposed study have the strong potential to impact ERCP practices worldwide, whether positive or negative.

Who can join: Review the eligibility criteria below.

Location: Peter Lougheed Centre โ€” Calgary, Alberta

Age range: 18 Years to 75 Years

๐Ÿงช Interventions in This Study

  • Intravenous Ringer's lactate (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • Peter Lougheed Centre โ€” Calgary, Alberta

๐Ÿ“ž Contact the Study Coordinator

Phone: (403) 880-8508

Email: nauzer.forbes@ucalgary.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Post-ERCP Acute Pancreatitis

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—