Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06860984

Evaluating the Safety and Efficacy of Duloxetine in the Prevention of Post Endoscopic Retrograde Cholangiopancreatography Pancreatitis

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
44 (estimated)
Sponsor
Tanta University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Endoscopic retrograde cholangiopancreatography (ERCP (, a key tool that is used in diagnosis and treatment of pancreato-biliary diseases. Post-ERCP pancreatitis (PEP) is the most common and serious complication that can occur following this procedure and can lead to significant morbidity and mortality. A variety of patient-related and procedure-related factors have been associated with higher rates of PEP.

Conditions

Interventions

TypeNameDescription
DRUGDuloxetineDuloxetine, a non-opioid neuromodulator, has been widely used to manage neuropathic pain. It possesses dual central and peripheral analgesic properties
OTHERPlacebo capsulePlacebo will have the same look and appearance of active comparator

Timeline

Start date
2025-03-10
Primary completion
2026-06-20
Completion
2026-07-10
First posted
2025-03-06
Last updated
2025-11-18

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06860984. Inclusion in this directory is not an endorsement.