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PPIs and Fat Absorption in CF and EPI

Primary Purpose

Pancreatic Insufficiency, Cystic Fibrosis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Omeprazole 40mg Capsule
Placebo oral capsule
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Insufficiency focused on measuring fat absorption, pancreatic enzyme

Eligibility Criteria

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

Inclusion Criteria:

  • Cystic fibrosis and pancreatic insufficiency (Fecal elastase <200 ug/g stool)
  • Age ≥12 years
  • In usual state of good health
  • Willing to participate in a four-month study with three visits

Exclusion Criteria:

  • Forced expiratory vital capacity at one second (FEV1) <40% predicted
  • Pregnancy or breast feeding
  • Other illness affecting growth or nutritional status
  • Unwillingness to continue their clinically established PERT dose for the duration of the study
  • Use of other medication that affects dietary fat absorption
  • Allergy to soy products
  • Allergy to safflower products
  • For subjects ≥18 years, celiac disease or allergy to gluten

Sites / Locations

  • Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Treatment Arm

Placebo Arm

Arm Description

Subjects will take omeprazole 40mg daily for 28 days, then undergo assessments of fat absorption.

Subjects will take a placebo daily for 28 days, then undergo assessments of fat absorption.

Outcomes

Primary Outcome Measures

Coefficient of fat absorption
Gold standard measurement of fat malabsorption

Secondary Outcome Measures

Duodenal pH
Change in duodenal pH as measured by the SmartPill
Fat absorption via Malabsorption Blood Test
Measurement of serum pentadecanoic acid and heptadecanoic acid

Full Information

First Posted
May 29, 2018
Last Updated
April 14, 2023
Sponsor
Children's Hospital of Philadelphia
Collaborators
Chiesi USA, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT03551691
Brief Title
PPIs and Fat Absorption in CF and EPI
Official Title
Proton Pump Inhibitors and Fat Absorption in Subjects With Cystic Fibrosis and Pancreatic Insufficiency
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
August 7, 2018 (Actual)
Primary Completion Date
November 2, 2022 (Actual)
Study Completion Date
November 2, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital of Philadelphia
Collaborators
Chiesi USA, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a clinical trial with a cross over design investigating the effect of the proton pump inhibitor omeprazole on fat malabsorption in subjects with cystic fibrosis and pancreatic insufficiency. Participants will be randomized to receive either omeprazole or placebo for 28 days, then cross over and receive omeprazole or placebo for another 28 days. Markers of fat absorption will be measured after each treatment course.
Detailed Description
Fat malabsorption contributes to poor nutritional status in people with cystic fibrosis (CF) and exocrine pancreatic insufficiency (EPI). Prescribing gastric acid-reducing agents such as proton pump inhibitors (PPIs) and histamine receptor antagonists (H2RAs) as an adjunct to pancreatic enzyme replacement therapy (PERT) to improve PERT efficacy and dietary fat absorption has become accepted clinical practice in CF, despite limited evidence to support the practice. Establishing the efficacy and true health benefit of acid suppression for nutritional status and outcomes in CF is particularly important in light of potential health risks and cost associated with long-term or even lifetime use of these medications. This study aims to characterize changes in fat malabsorption using the coefficient of fat absorption (CFA) as the primary endpoint in subjects who are on and off acid suppression with a PPI in addition to PERT. Additionally, the SmartPill® will be used to evaluate duodenal power of hydrogen (pH) while on and off acid suppression, and the malabsorption blood test (MBT) will be used to characterize changes in fat absorption. Associations will be explored between changes in nutritional status (weight, height, BMI), clinical GI symptoms, and quality of life in subjects treated with PPI vs. placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Insufficiency, Cystic Fibrosis
Keywords
fat absorption, pancreatic enzyme

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment Arm
Arm Type
Active Comparator
Arm Description
Subjects will take omeprazole 40mg daily for 28 days, then undergo assessments of fat absorption.
Arm Title
Placebo Arm
Arm Type
Placebo Comparator
Arm Description
Subjects will take a placebo daily for 28 days, then undergo assessments of fat absorption.
Intervention Type
Drug
Intervention Name(s)
Omeprazole 40mg Capsule
Intervention Description
Omeprazole 40mg daily for 28 days
Intervention Type
Drug
Intervention Name(s)
Placebo oral capsule
Intervention Description
Identically-appearing capsule to omeprazole
Primary Outcome Measure Information:
Title
Coefficient of fat absorption
Description
Gold standard measurement of fat malabsorption
Time Frame
After 28 days of treatment or placebo
Secondary Outcome Measure Information:
Title
Duodenal pH
Description
Change in duodenal pH as measured by the SmartPill
Time Frame
After 28 days of treatment or placebo
Title
Fat absorption via Malabsorption Blood Test
Description
Measurement of serum pentadecanoic acid and heptadecanoic acid
Time Frame
After 28 days of treatment or placebo

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cystic fibrosis and pancreatic insufficiency (Fecal elastase <200 ug/g stool) Age ≥12 years In usual state of good health Willing to participate in a four-month study with three visits Exclusion Criteria: Forced expiratory vital capacity at one second (FEV1) <40% predicted Pregnancy or breast feeding Other illness affecting growth or nutritional status Unwillingness to continue their clinically established PERT dose for the duration of the study Use of other medication that affects dietary fat absorption Allergy to soy products Allergy to safflower products For subjects ≥18 years, celiac disease or allergy to gluten
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginia A Stallings, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19146
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported will be shared upon request, after deidentification.
IPD Sharing Time Frame
The data will be available immediately upon publication.
IPD Sharing Access Criteria
Contact brownellj@email.chop.edu. Requestors will need to sign a data access agreement.
Citations:
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PPIs and Fat Absorption in CF and EPI

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