DRonabinol Treatment of OSA
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- VA Office of Research and Development
- Study ID
- NCT06477952
- Phase
- PHASE1/PHASE2
- Status
- Recruiting
Conditions
- Obstructive Sleep Apnea
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Dronabinol — DRUGOpen label Dronabinol treatment for two weeks.
Study Details
This is an open-label trial that tests the effectiveness of Dronabinol in treating obstructive sleep apnea (OSA). All participants will take oral Dronabinol for two weeks. Sleep studies will be conducted before and after treatment to measure OSA severity.
Key Dates
- Start date
- Aug 25, 2025
- Status verified
- Sep 2025
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Single groupOpen label Dronabinol treatment for two weeks.
Primary Outcome Measure
Apnea hypopnea index (AHI) [ Time Frame: 2 weeks ]
Central Contacts
- Bharati Prasad, MD(312) 996-8433
- Karen M Lenehan(312) 569-6343
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Jesse Brown VA Medical Center, Chicago, IL | Chicago | Illinois | 60612 | Bharati Prasad, MD (PRINCIPAL_INVESTIGATOR) |
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