ASA Triad Clinical Trial
Official title:
A Pilot Study of the Effectiveness of a High Omega-3/Low Omega-6 Treatment Diet for Treating Aspirin-exacerbated Respiratory Disease
NCT number | NCT02064738 |
Other study ID # | 2013-P002683 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 2014 |
Est. completion date | April 2017 |
Verified date | January 2019 |
Source | Brigham and Women's Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this trial is to test the hypothesis that a treatment diet low in omega-6 fatty acids and high in omega-3 fatty acids can cause improvement in asthma symptoms, nasal symptoms, and pulmonary function in patients with aspirin-exacerbated respiratory disease (AERD).
Status | Completed |
Enrollment | 10 |
Est. completion date | April 2017 |
Est. primary completion date | March 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - History of physician-diagnosed asthma - History of nasal polyposis - History of at least two reactions to oral aspirin or other nonselective cyclooxygenase inhibitor with features of lower airway involvement (cough, chest tightness, wheezing, dyspnea), or diagnosis of AERD via a physician-conducted challenge to aspirin - Age between 18 and 70 years Exclusion Criteria: - Current smoking, defined as daily tobacco smoking in the last 6 months and at least one instance of tobacco smoking in the last 3 months. - Current pregnancy or breastfeeding - BMI <20 - History of allergy to fish or any unwillingness to eat fish as a regular part of the diet - Use of Zyflo (zileuton) in the last two weeks - Presence of an implantable cardioverter-defibrillator - Use of oral steroids in the last two weeks - Participation in any other clinical trial in the last month - Any use of nonsteroidal antiinflammatory drugs (NSAIDs) or any drug that inhibits the cyclooxygenase enzyme during the course of the study |
Country | Name | City | State |
---|---|---|---|
United States | Brigham and Women's Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Brigham and Women's Hospital |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in urinary prostaglandin D2 level | 2 weeks and 4 weeks | ||
Other | Change in blood eosinophil count | 2 weeks and 4 weeks | ||
Other | Change in platelet-leukocyte aggregates | 2 weeks and 4 weeks | ||
Primary | Change in urinary leukotriene E4 levels | 2 weeks and 4 weeks | ||
Primary | Change in serum leukotriene B4 levels | 2 weeks and 4 weeks | ||
Secondary | Change in asthma control questionnaire score | Baseline, 2 weeks, and 4 weeks | ||
Secondary | Change in Sino-Nasal Outcome Test-22 (SNOT-22) score | Baseline, 2 weeks, and 4 weeks | ||
Secondary | Change in forced expiratory volume in one second (FEV1), forced vital capacity (FVC), and FEV1/FVC | Baseline, two weeks, and four weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
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