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IV Ibuprofen for the Prevention of Post-ERCP Pancreatitis

Primary Purpose

Post-ERCP Acute Pancreatitis

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Ibuprofen
placebo
Sponsored by
University of Texas Southwestern Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Post-ERCP Acute Pancreatitis focused on measuring post-ERCP pancreatitis, pediatric, ibuprofen

Eligibility Criteria

undefined - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

  • Age>18
  • Pancreatitis within the 72 hours preceding ERCP
  • Allergy or hypersensitivity to Aspirin or NSAID medications
  • Pregnancy or breastfeeding mother
  • Cr >1.4
  • Gastrointestinal hemorrhage in preceding 72 hours
  • Heart disease reliant upon a patient ductus arteriosis
  • History of sickle cell disease

Sites / Locations

  • Children's Medical Center of Dallas

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Ibuprofen

Placebo

Arm Description

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

Single dose IV normal saline

Outcomes

Primary Outcome Measures

Post-ERCP Pancreatitis
Number of patients who develop post-ERCP pancreatitis

Secondary Outcome Measures

Post-ERCP Bleeding
Number of patients who develop post-ERCP bleeding

Full Information

First Posted
September 11, 2014
Last Updated
February 5, 2020
Sponsor
University of Texas Southwestern Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02241512
Brief Title
IV Ibuprofen for the Prevention of Post-ERCP Pancreatitis
Official Title
IV Ibuprofen for the Prevention of Post-ERCP Pancreatitis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Terminated
Why Stopped
lack of funding
Study Start Date
September 2014 (undefined)
Primary Completion Date
September 2018 (Actual)
Study Completion Date
September 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-ERCP Acute Pancreatitis
Keywords
post-ERCP pancreatitis, pediatric, ibuprofen

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
69 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ibuprofen
Arm Type
Experimental
Arm Description
Single dose IV Ibuprofen at a dose of 10mg/kg (max: 800mg).
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Single dose IV normal saline
Intervention Type
Drug
Intervention Name(s)
Ibuprofen
Other Intervention Name(s)
Caldolor
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
Normal Saline
Primary Outcome Measure Information:
Title
Post-ERCP Pancreatitis
Description
Number of patients who develop post-ERCP pancreatitis
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Post-ERCP Bleeding
Description
Number of patients who develop post-ERCP bleeding
Time Frame
2 weeks
Other Pre-specified Outcome Measures:
Title
Increased Pain Score
Description
Number of patients with increased pain scores after the procedure
Time Frame
pre-procedural, 24 hours
Title
24-h Post-ERCP Pain Score
Description
Pain score recorded 24-hrs after the ERCP was performed as recorded on a 10-point Likert pain scale (0= lowest value, no pain, 10=highest value, severe pain)
Time Frame
pre-procedural, 24 hours

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age<=18 years Undergoing ERCP (defined as cannulation of the major or minor papilla) for any indication Exclusion Criteria: Age>18 Pancreatitis within the 72 hours preceding ERCP Allergy or hypersensitivity to Aspirin or NSAID medications Pregnancy or breastfeeding mother Cr >1.4 Gastrointestinal hemorrhage in preceding 72 hours Heart disease reliant upon a patient ductus arteriosis History of sickle cell disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David M Troendle, MD
Organizational Affiliation
UT Southwestern Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Medical Center of Dallas
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
31651801
Citation
Troendle DM, Gurram B, Huang R, Barth BA. IV Ibuprofen for Prevention of Post-ERCP Pancreatitis in Children: A Randomized Placebo-controlled Feasibility Study. J Pediatr Gastroenterol Nutr. 2020 Jan;70(1):121-126. doi: 10.1097/MPG.0000000000002524.
Results Reference
derived

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IV Ibuprofen for the Prevention of Post-ERCP Pancreatitis

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