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Clinical Trials/NCT02241512
NCT02241512
Terminated
Phase 2

IV Ibuprofen for the Prevention of Post-ERCP Pancreatitis

University of Texas Southwestern Medical Center1 site in 1 country69 target enrollmentSeptember 2014

Overview

Phase
Phase 2
Intervention
Ibuprofen
Conditions
Post-ERCP Acute Pancreatitis
Sponsor
University of Texas Southwestern Medical Center
Enrollment
69
Locations
1
Primary Endpoint
Post-ERCP Pancreatitis
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

Endoscopic retrograde cholangiopancreatography (ERCP) is an advanced endoscopic technique utilized to diagnose and treat pathologic conditions involving the ducts draining the liver and pancreas. Post-ERCP pancreatitis (PEP) is the most common complication following ERCP and occurs in approximately 11% of children undergoing the procedure. By definition it leads to prolongation of hospital stay or delays in care and rarely can result in long-term morbidity or even death. Recent adult trials have demonstrated prevention of PEP with administration of rectal nonsteroidal anti-inflammatory drugs (NSAIDS). To date, no studies have been performed in children thus no "gold standard" or even commonly accepted method of preventing PEP in the pediatric population exist. Studying an IV NSAID such as ibuprofen has distinct advantages over rectally administered NSAIDs in the pediatric population in that it would allow for more consistent weight based dosing and would have more predictable absorption compared to suppository. Thus, this project proposes a pilot study evaluating the effectiveness of IV ibuprofen at preventing PEP in the pediatric population. The design of the proposed study is a prospective randomized double-blind trial comparing IV Ibuprofen to placebo controls (normal saline) at the time of procedure in patients undergoing ERCP at Children's Medical Center Dallas over a two-year period. The primary outcome measurement will be development of PEP. Post-ERCP bleeding and change in pre- and post- procedural pain scores will also be measured. The hypothesis is that IV Ibuprofen administered at the time of ERCP will decrease rates of post-ERCP pancreatitis in pediatric patients.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
September 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

David M Troendle

Dr.

University of Texas Southwestern Medical Center

Eligibility Criteria

Inclusion Criteria

  • Age\<=18 years
  • Undergoing ERCP (defined as cannulation of the major or minor papilla) for any indication

Exclusion Criteria

  • Pancreatitis within the 72 hours preceding ERCP
  • Allergy or hypersensitivity to Aspirin or NSAID medications
  • Pregnancy or breastfeeding mother
  • Gastrointestinal hemorrhage in preceding 72 hours
  • Heart disease reliant upon a patient ductus arteriosis
  • History of sickle cell disease

Arms & Interventions

Ibuprofen

Single dose IV Ibuprofen at a dose of 10mg/kg (max: 800mg).

Intervention: Ibuprofen

Placebo

Single dose IV normal saline

Intervention: placebo

Outcomes

Primary Outcomes

Post-ERCP Pancreatitis

Time Frame: 2 weeks

Number of patients who develop post-ERCP pancreatitis

Secondary Outcomes

  • Post-ERCP Bleeding(2 weeks)

Study Sites (1)

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