Ganglion Cyst Clinical Trials

Find Ganglion Cyst Clinical Trials Near You

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

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 18 years or older

• PTSD (PCL Score of 33 or greater at baseline screening)

• Willing and able to provide informed consent and complete study procedures

• Fluent in English

• Special Operations Forces Veteran

Locations
United States
Ohio
Reset Medical and Wellness Center
RECRUITING
Strongsville
Contact Information
Primary
Michael Louwers, MD
mlouwers@theresetcenter.com
877-737-3810
Time Frame
Start Date: 2026-03-20
Estimated Completion Date: 2027-07-01
Participants
Target number of participants: 75
Treatments
Ropivacaine Based BCSB
This cohort consists of combat veterans participating in the RESET study to evaluate the effects of bilateral cervical sympathetic ganglion blocks (BCSB) on post-traumatic stress symptoms and suicide risk. Participants receive one procedures as a clinical intervention. Some participants may decided to access additional therapies, making BCSB an integrative model.
Sponsors
Leads: Reset Medical and Wellness Center

This content was sourced from clinicaltrials.gov