NCT07087015View on ClinicalTrials.gov

Efficacy of Cervical Sympathetic Blocks for PTSD

NANot yet recruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

October 31, 2025

Primary Completion Date

December 31, 2026

Study Completion Date

December 31, 2026

Conditions
PTSD
Interventions
PROCEDURE

Cervical sympathetic nerve block

Patients will receive a CSB.

PROCEDURE

Subcutaneous sham injection

Patients will receive a subcutaneous sham injection of saline.

DRUG

Ropivacaine

The CSB group will receive ropivacaine 0.5% 10ml.

DRUG

Normal Saline

The control group will receive 3 ml of normal saline in the sham injection.

All Listed Sponsors
lead

Stanford University

OTHER

NCT07087015 - Efficacy of Cervical Sympathetic Blocks for PTSD | Biotech Hunter | Biotech Hunter