Actively Recruiting
Monitoring Patients With Repetitive Head Impact With Gamma-glutamylcysteine Supplementation
Led by Pravat Mandal · Updated on 2026-04-09
30
Participants Needed
1
Research Sites
90 weeks
Total Duration
On this page
Sponsors
P
Pravat Mandal
Lead Sponsor
C
Chuck Noll Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to test whether the gamma - glutamylcystiene (GGC) oral supplement can reach the brain and subsequently increase antioxidant glutathione (GSH) level in people with repetitive head impact (RHI). This will reduce the oxidative stress related injury in people with RHI.This unique study's main objective is to test the: 1. Change in GSH in brain and blood levels through GGC supplementation. 2. Change in the cognitive function in RHI patients due to GGC supplementation.
CONDITIONS
Official Title
Monitoring Patients With Repetitive Head Impact With Gamma-glutamylcysteine Supplementation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Retired NFL player, retired Navy SEAL, or army personnel with combat experience exposed to repetitive head impact
- Self- or informant-reported memory or behavioral complaints
- Age between 30 and 70 years
- Able to read, write English, and give consent to participate
You will not qualify if you...
- Presence of pacemakers, aneurysm clips, artificial heart valves, ear implants, or metal fragments in the eyes, skin, or body
- Claustrophobia
- Mild cognitive impairment defined by TICS score 29 or lower or 1 or more standard deviations below age expectation on two or more cognitive tests in the same domain
- History of cancer
- Active psychosis or delirium
- Chronic kidney disease (creatinine > 1.5 mg/dL) or liver disease (AST or ALT ≥ 1.5 times upper limit of normal) within 30 days before enrollment
- Use of antioxidant therapy (gingko biloba or N-acetylcysteine) or illicit drug abuse/dependence
- Neurosurgical intervention due to repeated head injury
- Repeated head injury within the last 90 days
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UPMC Presbyterian Hospital
Pittsburgh, Pennsylvania, United States, 15213
Actively Recruiting
Research Team
P
Pravat K MANDAL, PHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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