RecruitingPhase 2NCT06608277

Ketamine, SGB and Combination Treatment for TBI-associated Headache or PTSD

Multi-Center, Randomized, Double-Blind, Placebo-Controlled Trial Comparing Ketamine, Stellate Ganglion Blocks and Combination Treatment to Sham Therapies for Traumatic Brain Injury-Associated Headaches and Post-Traumatic Stress Disorder


Sponsor

Northwestern University

Enrollment

175 participants

Start Date

Jul 2, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Post-Traumatic Stress Disorder (PTSD) and traumatic brain injury (TBI) with associated headache are amongst the most common injuries sustained by our deployed forces in Iraq and Afghanistan, as well as in more recent conflicts in Eastern Europe and the Middle East. This study aims to determine whether a procedural intervention (stellate ganglion block (SGB)) or medication (ketamine), alone or in combination, can alleviate PTSD and TBI-associated headache. Determining efficacious treatments in a randomized, double-blind, placebo-controlled, multicenter study trial may improve quality of life in those with TBI and PTSD, and identifying factors associated with treatment outcome (personalized medicine) may enhance selection, thereby improving the risk: benefit and cost-effectiveness ratios. Primary Objectives: 1. To determine the efficacy of SGB and ketamine infusion as stand-alone treatments for TBI-related headache; 2. To determine the efficacy of SGB and ketamine infusion as stand-alone treatments for PTSD; 3. To determine the comparative effectiveness of SGB and ketamine infusion, and the effect of combination treatment on TBI-related headache and PTSD; 4. Exploratory Aim 1: To determine the effects of SGB, ketamine infusion, and the combination on structural and functional MRI, biomarker levels and pain thresholds and tolerance; 5. Exploratory Aim 2: To identify factors associated with treatment responders overall and for individual treatment groups. Secondary Objectives: 1. Exploratory Aim 1: To determine the effects of SGB, ketamine infusion, and the combination on structural and functional MRI, biomarker levels and pain thresholds and tolerance (Biomedical levels and MRI not included at Northwestern University Site). 2. Exploratory Aim 2: To identify factors associated with treatment responders overall and for individual treatment groups.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing three treatments for people living with traumatic brain injury (TBI) and/or post-traumatic stress disorder (PTSD): ketamine infusions, a nerve block procedure called a stellate ganglion block (SGB), and a combination of both. Researchers want to find out which approach works best for chronic headaches and PTSD symptoms. **You may be eligible if...** - You are 18 years or older - You have been living with TBI-related headaches and/or PTSD for more than 3 months - Your symptoms score high enough on validated symptom scales - Your medications have been stable for more than 2 weeks **You may NOT be eligible if...** - You have had a ketamine infusion or stellate ganglion block in the past 6 months - You have serious medical or mental health conditions beyond TBI or PTSD (e.g., dementia, Parkinson's disease) - You have increased pressure in the brain - You had pre-existing headaches before your TBI that explain the headache severity Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREGroup A active comparator

Group A placebo comparator. Stellate Ganglion Block plus placebo (.9 normal saline) infusion

DRUGGroup B active comparator

Active Comparator: Group B = Sham Stellate Ganglion Block plus ketamine infusion

COMBINATION_PRODUCTGroup C Experimental

Group C experimental Stellate Ganglion Block plus ketamine infusion

OTHERGroup D Placebo Comparator

Group D Placebo Comparator: Sham Stellate Ganglion Block plus placebo normal saline


Locations(3)

Anesthesiology Pain Medicine Center

Chicago, Illinois, United States

Walter Reed National Military Medical Center

Bethesda, Maryland, United States

Womack Army Medical Center

Fort Bragg, North Carolina, United States

View Full Details on ClinicalTrials.gov

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NCT06608277


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