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Trials / Recruiting

RecruitingNCT06260878

Short-term Intravenous Fluids for Prevention of Post-ERCP Pancreatitis

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
505 (estimated)
Sponsor
University of Calgary · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
OTHERIntravenous Ringer's lactateIntravenous Ringer's lactate

Timeline

Start date
2024-11-22
Primary completion
2027-12-31
Completion
2028-06-30
First posted
2024-02-15
Last updated
2024-12-20

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06260878. Inclusion in this directory is not an endorsement.

Short-term Intravenous Fluids for Prevention of Post-ERCP Pancreatitis (NCT06260878) · Clinical Trials Directory