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
| Type | Name | Description |
|---|---|---|
| OTHER | Intravenous Ringer's lactate | Intravenous 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.