← Back to Search

Antibiotic

Hypertonic Saline for Nontuberculous Mycobacterial Lung Disease

Phase 4
Recruiting
Research Sponsored by Oregon Health and Science University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age 18 and older
At least 2 positive MAC sputum cultures in the last 12 months with at least one AFB positive sputum obtained within 12 weeks prior to randomization
Must not have
Current use of chronic systemic corticosteroids at doses of 15 mg/day for more than 3 months
Diagnosis of HIV
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 weeks
Awards & highlights

Summary

This trial is testing whether inhaling a saltwater solution can help patients with a specific lung infection by making it easier to clear mucus from their lungs. Saltwater solutions have been used to improve mucus clearance in conditions like cystic fibrosis and chronic bronchitis.

Who is the study for?
This trial is for adults over 18 with M. avium complex lung infections who meet specific lung disease criteria and have had at least two positive MAC sputum cultures in the past year. It's not for those with HIV, cystic fibrosis, certain NTM diseases, active tuberculosis or fungal infections, high-dose steroid users, organ transplant recipients, or anyone unable to consent.
What is being tested?
The study examines if inhaling hypertonic saline can help reduce symptoms and improve mycobacteria clearance in patients with M. avium complex lung disease. Participants will also receive standard treatments like Azithromycin, Ethambutol, and Rifampin.
What are the potential side effects?
Potential side effects may include irritation of the airways from hypertonic saline inhalation leading to coughing or wheezing; gastrointestinal issues from Azithromycin; vision problems or stomach pain from Ethambutol; and liver issues or flu-like symptoms from Rifampin.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am 18 years old or older.
Select...
I have had at least 2 positive lung infection tests in the last year.
Select...
I have been diagnosed with Bronchiectasis or it has been seen on my chest CT.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I have been taking more than 15 mg/day of corticosteroids for over 3 months.
Select...
I have been diagnosed with HIV.
Select...
I have been diagnosed with Cystic Fibrosis.
Select...
My condition involves lung cavities due to NTM infection.
Select...
I am currently being treated for active tuberculosis or a serious fungal infection.
Select...
I have had a lung or other solid organ transplant.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Culture conversion
Secondary study objectives
Semi-quantitative culture results

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Hypertonic salineExperimental Treatment1 Intervention
Patients who randomize to the hypertonic saline arm will be prescribed a nebulizer device to nebulize hypertonic saline (7%) twice daily for 12 weeks. Hypertonic saline (3%) can be prescribed in the case of poor tolerability of the 7% solution.
Group II: Standard of CareActive Control3 Interventions
Patients who randomize to the standard of care arm will receive treatment for pulmonary MAC based on the approved ATS/IDSA guidelines. Changes to standard of care regimen may be made based on the investigator's discretion.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Hypertonic saline
2017
Completed Phase 4
~1320

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Nontuberculous Mycobacterial (NTM) Lung Disease include antibiotics such as macrolides, rifamycins, and ethambutol, which work by inhibiting bacterial protein synthesis, RNA synthesis, and cell wall synthesis, respectively. Hypertonic saline, a treatment under study, draws water out of lung tissues to thin mucus, aiding in the clearance of mycobacteria. This is crucial for NTM patients as it helps reduce bacterial load and improve lung function by enhancing mucociliary clearance, thereby alleviating symptoms and potentially improving clinical outcomes.
[Study of the mucociliary transport rate in evaluating the effectiveness of the treatment of suppurative endobronchitis by CO2 laser].Nebulised hypertonic saline for cystic fibrosis.The long and winding road to inhaled TB therapy: not only the bug's fault.

Find a Location

Who is running the clinical trial?

New York UniversityOTHER
234 Previous Clinical Trials
313,845 Total Patients Enrolled
Oregon Health and Science UniversityLead Sponsor
994 Previous Clinical Trials
7,386,898 Total Patients Enrolled
NTM Info & Research, Inc.UNKNOWN

Media Library

Azithromycin (Antibiotic) Clinical Trial Eligibility Overview. Trial Name: NCT04921943 — Phase 4
Nontuberculous Mycobacterial Lung Disease Research Study Groups: Hypertonic saline, Standard of Care
Nontuberculous Mycobacterial Lung Disease Clinical Trial 2023: Azithromycin Highlights & Side Effects. Trial Name: NCT04921943 — Phase 4
Azithromycin (Antibiotic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04921943 — Phase 4
~9 spots leftby Jun 2025