Clinical trials

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Condition / disease
Location
Status: Recruiting

Integrative Bilateral Cervical Sympathetic Blocks for Trauma-Related Symptoms in Special Operations Veterans: A Prospective Case Series

This study prospectively evaluates the effects of Integrative Bilateral Cervical Sympathetic Block (BCSB) on trauma-related symptoms in Special Operations Veterans, comparing outcomes in those receiving BCSB alone versus BCSB combined with structured integrative therapy. Using standardized FDA-approved dosing, validated symptom measures, and strict safety criteria, the study aims to determine whether this dual-level autonomic intervention improves PTSD-related and TBI-related symptoms, and whether pairing the procedure with therapy enhances durability and overall clinical benefit.

Participants needed: 75
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Reset Medical and Wellness CenterUpdated: Mar 20, 2026Locations: 1Duration: 270 Days
Eligibility criteria

18 years or older [+4]

Recent Sympathetic Block: Receipt of any cervical sympathetic block (including s... [+5]