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Clinical Trials in Canada / NCT05211206
Recruiting Observational

IV Fluids and Post-ERCP Pancreatitis

NCT05211206 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2022-01-10
Last updated
2026-04-29

Condition(s) studied

ERCP

Investigational drug(s) / intervention(s)

IV fluids

IV fluids: Amount of intravenous fluids delivered

Study summary

Aggressive intravenous hydration has been shown in randomized trials to prevent post-endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis (PEP), though studied regimens are often impractical. To date, no studies have prospectively assessed short-term (60-90 minute) aggressive hydration regimens that are feasible for outpatients undergoing ERCP and subsequent discharge. Furthermore, little is known with regard to fluid type, volume, and timing with respect to ERCP. In this study, we will aim to assess whether the amount of peri-procedural intravenous fluid administered around the time of ERCP is associated with the risk of PEP (the primary outcome).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Subject referred for ERCP, regardless of indication; * Subject age 18 years or older; * Subject able to give informed consent to involvement be included. Exclusion Criteria: * Subject has a standard contraindication to ERCP; * Subject or surrogate unable or unwilling to provide informed consent; * Subject age \< 18 years.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peter Lougheed Hospital Calgary Alberta Recruiting

More University of Calgary trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05211206 on ClinicalTrials.gov ↗ ← All trials in Canada