The Role of GER in Exercise Triggered Asthma
Primary Purpose
Asthma
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Achipex
Sponsored by

About this trial
This is an interventional diagnostic trial for Asthma focused on measuring Asthma
Eligibility Criteria
Inclusion Criteria: Exercise-triggered asthmatics - defined as asthmatics with exertion as their primary exacerbating factor and experiencing less than two episodes of classic gastroesophageal reflux a week. Exclusion Criteria: Exclusion criteria will be the following: Severe asthma (recent or repeated hospitalizations) Severe angina, cardiac arrhythmia's, heart failure, prior MI Respiratory illness e.g. COPD Inability to receive therapy/pH probe Pregnancy Minors, prisoners, individuals unable to give informed consent Prior upper GI surgery (gastrectomy, etc)
Sites / Locations
- University of Utah
Outcomes
Primary Outcome Measures
To determine whether patients with exercise-triggered asthma experience GER during exercise.
Secondary Outcome Measures
To determine whether the exercise-induced GER within the subjects relates temporally to their exertional asthma.
Full Information
NCT ID
NCT00204672
First Posted
September 12, 2005
Last Updated
September 12, 2005
Sponsor
University of Utah
Collaborators
PriCara, Unit of Ortho-McNeil, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT00204672
Brief Title
The Role of GER in Exercise Triggered Asthma
Official Title
The Role of GER in Exercise Triggered Asthma
Study Type
Interventional
2. Study Status
Record Verification Date
September 2005
Overall Recruitment Status
Completed
Study Start Date
October 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2005 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
University of Utah
Collaborators
PriCara, Unit of Ortho-McNeil, Inc.
4. Oversight
5. Study Description
Brief Summary
HYPOTHESIS
Gastroesophageal reflux is a major contributor to exercise-triggered asthma.
Two groups of patients will be studied: those with asthma who have difficulty with exertion, those without asthma who experience difficulty with exertion. Both groups will experience gastroesophageal reflux (GER) twice of less per week. Patients will complete a treadmill exam to determine their VO2 max. They will then undergo pH monitoring while exercising for 30 minutes at 65-70% of their VO2 max. Subjects will be given placebo or acid suppression pill for 12 weeks. At the end of 12 weeks, the subjects will repeat the exercise (30 minutes) and 24-hour pH study.
Detailed Description
PRIMARY OBJECTIVE
To determine whether patients with exercise-triggered asthma experience GER during exercise.
SECONDARY OBJECTIVES
To determine whether the exercise-induced GER within the subjects relates temporally to their exertional asthma.
To evaluate the efficacy of potent acid suppression with a proton pump inhibitor in suppressing exercise-triggered GER and asthma in these subjects.
METHODS
Population to be evaluated:
Exercise-triggered asthmatics - defined as asthmatics with exertion as their primary exacerbating factor and experiencing less than two episodes of classic gastroesophageal reflux a week.
These patients will be randomized into three different treatment groups:
Placebo BID
20 mg Aciphex QD and placebo QPM
20 mg Aciphex BID
12 patients will be studied in each group.
DATA
pH data - Data will be collected on the frequency and duration of the reflux episodes (number of episodes and the percent time the esophageal pH is less than 4.0). This will then be correlated with the respiratory symptom and changes in spirometry. A symptom index will be designed to associate the episodes of reflux and bronchospasm that occur within 5 minutes of a drop in esophageal pH.
Exercise Tolerance/Symptoms - comparisons will be made between the three groups regarding symptomatology during exercise after randomization to either placebo or differing doses of Aciphex.
Spirometry testing - done after exercise test. Comparisons between baseline and following treatment Symptoms scores - both the overall numerical grades of the patients quality of life and the number of asthmatic episodes and rescue inhaler use will be compared to baseline after the 12 week study.
STUDY DURATION
The asthma database at the University covers approximately 500 patients. A database search will be performed to identify patients suitable for recruitment. Additional recruitment, if needed, will be pursued through radio advertising. Once the study is initiated, the baseline time for therapy is 12 weeks for each patient. An estimate of the time necessary to complete the study is 15 months.
STATISTICS
Exercise triggered asthma has not been well studied with respect to its relationship to GER. This study will be considered a pilot study with 12 subjects per arm. Results from this study may be used to power a follow up study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Asthma
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
36 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Achipex
Primary Outcome Measure Information:
Title
To determine whether patients with exercise-triggered asthma experience GER during exercise.
Secondary Outcome Measure Information:
Title
To determine whether the exercise-induced GER within the subjects relates temporally to their exertional asthma.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Exercise-triggered asthmatics - defined as asthmatics with exertion as their primary exacerbating factor and experiencing less than two episodes of classic gastroesophageal reflux a week.
Exclusion Criteria:
Exclusion criteria will be the following:
Severe asthma (recent or repeated hospitalizations)
Severe angina, cardiac arrhythmia's, heart failure, prior MI
Respiratory illness e.g. COPD
Inability to receive therapy/pH probe
Pregnancy
Minors, prisoners, individuals unable to give informed consent
Prior upper GI surgery (gastrectomy, etc)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathryn A Peterson, M.D.
Organizational Affiliation
University of Utah
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84132
Country
United States
12. IPD Sharing Statement
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The Role of GER in Exercise Triggered Asthma
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