Paclitaxel-Coated Pulmonary Balloon for the Treatment of Benign Central Airway Stenosis
Part of paid clinical trials in Baltimore, Maryland.
- Sponsor
- Airiver Medical, Inc.
- Study ID
- NCT07191860
- Status
- Recruiting
Conditions
- Adult Benign Central Airway Stenosis
- Adult Subjects With Symptomatic Benign Airway Obstruction
- Adult Tracheobronchial Stenosis
- Central Airway Obstruction
- Central Airway Stenosis
- Tracheal Stenosis
Eligibility Criteria
- Sex
- ALL
- Age
- 22 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- The Airiver Pulmonary drug-coated balloon (DCB) dilation — COMBINATION_PRODUCTdrug coated balloon dilation
- Commercial airway balloon dilation — DEVICEuncoated airway balloon dilation
Study Details
The OXYGEN-RCT trial is a randomized, controlled, double blinded, prospective, multi-center trial to demonstrate the safety and efficacy in adult benign central airway stenosis. Participates will be in a 1:1 allocation to treatment with the Airiver Pulmonary DCB or standard of care laryngoscopic/bronchoscopic balloon dilation, respectively.
Key Dates
- First listed
- Sep 25, 2025
- Start date
- Feb 24, 2026
- Status verified
- Dec 2025
- Primary completion
- Nov 1, 2027
- Completion
- Nov 1, 2030
Study Design
- Enrollment
- 200 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: treatment with the Airiver Pulmonary DCBdilate benign stenoses of the airway tree.
- Active Comparator: treatment of Commercial airway dilation balloondilate benign stenoses of the airway tree.
Primary Outcome Measure
Primary Safety: defined as Incidence of device- and/or procedure-related Major Adverse Events(MAEs) [ Time Frame: 30 days post index procedure ]
Central Contacts
- Robyn Schacherer, RN6123108755
- Mitch Erickson6518954399
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Johns Hopkins University | Baltimore | Maryland | 21218 |
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