Beta-Blocker Influences on Inflammatory and Neural Responses to Stress
Part of paid clinical trials in Chapel Hill, North Carolina.
- Sponsor
- University of North Carolina, Chapel Hill
- Study ID
- NCT06263452
- Phase
- PHASE4
- Status
- Recruiting
Conditions
- Cardiovascular Disease
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 30 Years
- Healthy Volunteers
- Accepted
Interventions
- Propranolol — DRUGTablet encapsulated to visually look identical to the placebo.
- Placebo — DRUGEncapsulated sugar pill to visually look identical to the experimental condition.
Study Details
The purpose of this study is to map the neural and molecular mechanisms underlying psychological stress-induced changes in inflammation which could reveal new targets for intervention to reduce the risk of cardiovascular disease.
Key Dates
- Start date
- May 1, 2024
- Status verified
- Oct 2025
- Primary completion
- May 31, 2026
- Completion
- May 31, 2026
Study Design
- Enrollment
- 120 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- BASIC_SCIENCE
Arms
- Experimental: PropranololPropranolol tablet, 40mg, one-time, orally
- Placebo Comparator: PlaceboEncapsulated placebo tablet
Primary Outcome Measure
Change in levels of pro-inflammatory cytokine interleukin-6 in response to social stress [ Time Frame: Post-drug baseline to 90-minutes post-stress task (T-90) ]
Central Contacts
- Jonathan Bunting, BS9164957661
- Keely A Muscatell, PhD9164957661
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Social Neuroscience and Health Laboratory | Chapel Hill | North Carolina | 27514 | Jessica R Cohen, PhD (SUB_INVESTIGATOR) Kristen A Lindquist, PhD (SUB_INVESTIGATOR) Zev Nakamura, MD (SUB_INVESTIGATOR) |
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