Hypertonic Saline for MAC
Start Date
5/18/2021
Completion Date
12/31/2025
Summary
The MAC-HS study is a testing whether hypertonic saline helps improve symptoms and clearance of mycobacteria in patients with M. avium complex lung infections.
Detailed Description
The MAC-HS study is an open label, randomized control trial of hypertonic saline in pulmonary M. avium complex patients. Eligible patients who consent to participate will be randomized 1:1 to hypertonic saline or standard of care for 12 weeks. All patients in the treatment group will take inhaled hypertonic saline twice daily for 12 weeks. Patients may continue with other airway clearance methods (i.e. flutter, acapella valve, aerobika, postural drainage, huff cough, percussion). Patients may also be treated with antibiotics targeted at other pathogens if an exacerbation occurs. Patients may also be actively treated with inhaled corticosteroid at the time of enrollment, with dosing adjustments during the trial discouraged. Patients with disease progression at any time can be discontinued from the study treatment and treated according to ATS/IDSA guidelines at the discretion of the primary investigator. However, such patients will still complete the 12 week final visit, sputum collection and AE assessment.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Hypertonic saline
Azithromycin
Ethambutol
Rifampin
Conditions
Locations
NYU Langone Health
New York, New York 10016
United States
Oregon Health & Science University
Portland, Oregon 97239
United States
University Health Network
Toronto, Ontario ON M5G
Canada