Metformin Hydrochloride Extended-Release Tablets
Drugtitrated to 2000 mg once daily
NCT Number: NCT06273072
This is a randomized clinical trial of metformin among overweight or obese adults with not well-controlled asthma despite maintenance inhaler therapy.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Johns Hopkins University, Baltimore, Maryland, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
titrated to 2000 mg once daily
placebo
Time frame: Baseline to week 24
Number of participants completing at least 3 out of the 4 monitoring telemedicine visits
Time frame: Baseline to week 24
Adherence will be measured by pill count
Time frame: Baseline to week 24
Investigators will collect data on the number of subjects screened, randomized, and complete the final in-person visit
Time frame: Baseline to week 24
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 (annualized) asthma exacerbations rate at week 24
Time frame: Baseline to week 24
Difference in volume of air exhaled in the first second during spirometry (FEV1) at week 24
Time frame: Baseline to week 24
Difference in FeNO between baseline and week 24
Time frame: Baseline to week 24
Difference in cumulative dose of mannitol required to precipitate a significant decrement in FEV1 between baseline at week 24
Contact information is provided by the study sponsor or research team.
Meredith C McCormack, M.D., M.H.S.
CONTACT
Rachelle Koehl, M.S.
CONTACT
Johns Hopkins University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05226416
Anemia, Arrhythmias, Cardiac
Moscow, Russia
View Trial DetailsNCT07536256
Adolescent Asthma, Asthma
Waianae, Hawaii, United States
View Trial DetailsNCT02575326
Asthma, Body Weight
Detroit, Michigan, United States
View Trial DetailsNCT00634036
Asthma, Body Weight
Pittsburgh, Pennsylvania, United States
View Trial Details