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Stellate Ganglion Block for Post-Traumatic Stress Disorder
Phase < 1
Waitlist Available
Led By Alan Peterson, PhD, ABPP
Research Sponsored by The University of Texas Health Science Center at San Antonio
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 1 month and 3 months
Awards & highlights
Study Summary
This trial is testing a new treatment for PTSD that combines exposure therapy with a stellate ganglion block injection.
Eligible Conditions
- Post-Traumatic Stress Disorder
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 1 month and 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 1 month and 3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in CAPS-5 (Clinician-Administered PTSD Scale)
Change in PCL-5 (Posttraumatic Stress Disorder Checklist)
Secondary outcome measures
Change in Brief Inventory of Psychosocial Functioning
Change in GAD-7 (General Anxiety Disorder Screener)
Change in PHQ-9 (Patient Health Questionnaire-9)
+1 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Stellate Ganglion BlockExperimental Treatment1 Intervention
One time administration of a stellate ganglion block
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Ropivacaine
FDA approved
Find a Location
Who is running the clinical trial?
The University of Texas Health Science Center at San AntonioLead Sponsor
452 Previous Clinical Trials
91,398 Total Patients Enrolled
United States Department of DefenseFED
864 Previous Clinical Trials
327,587 Total Patients Enrolled
Alan Peterson, PhD, ABPPPrincipal InvestigatorUniversity of Texas Health San Antonio Texas at San Antonio
2 Previous Clinical Trials
64 Total Patients Enrolled
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