This is a randomized clinical trial of metformin among overweight or obese adults with not well-controlled asthma despite maintenance inhaler therapy.
This is a randomized, placebo-controlled, parallel-arm pilot clinical trial. Adult participants who are overweight or obese and have not well-controlled asthma despite use of an inhaled corticosteroid will be randomized to metformin, an FDA-approved medication for the treatment of type 2 diabetes mellitus, or to placebo, to be taken daily for a total duration of six months. Recruitment will occur at two sites in the United States. Randomized participants will have regular telemedicine visits to assess side effects and adherence. Additionally, participants will have a measurement of asthma outcomes at randomization and at 3 and 6 months after randomization. The purpose of this study is to determine feasibility to inform a future multi-center clinical trial of metformin in this population.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
100
titrated to 2000 mg once daily
Johns Hopkins University
Baltimore, Maryland, United States
RECRUITINGBaylor College of Medicine
Houston, Texas, United States
RECRUITINGNumber of completed telemedicine visits
Number of participants completing at least 3 out of the 4 monitoring telemedicine visits
Time frame: Baseline to week 24
Adherence to study drug
Adherence will be measured by pill count
Time frame: Baseline to week 24
Retention rate
Investigators will collect data on the number of subjects screened, randomized, and complete the final in-person visit
Time frame: Baseline to week 24
Asthma control as assessed by the Asthma Control Test (ACT) score
Difference in Asthma Control Test (ACT) score at week 24; range is from 5-25 with higher being better asthma control
Time frame: Baseline to week 24
Change in Asthma exacerbations rate
Change in (annualized) asthma exacerbations rate at week 24
Time frame: Baseline to week 24
Pre-bronchodilator lung function
Difference in volume of air exhaled in the first second during spirometry (FEV1) at week 24
Time frame: Baseline to week 24
Fractional exhaled nitric oxide (FeNO)
Difference in FeNO between baseline and week 24
Time frame: Baseline to week 24
Airways hyperresponsiveness
Difference in cumulative dose of mannitol required to precipitate a significant decrement in FEV1 between baseline at week 24
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Time frame: Baseline to week 24