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Glutathione vs. Curcumin Clinical Trial

Testing the Model: A Phase I/II Randomized Double Blind Placebo Control Trial of Targeted Therapeutics: Liposomal Glutathione and Curcumin

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02848417
Acronym
Glutathione
Enrollment
75
Registered
2016-07-28
Start date
2016-04-30
Completion date
2020-08-31
Last updated
2020-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gulf War Syndrome

Brief summary

The investigator proposes to perform a phase I/II study comparing two nutraceuticals and placebo that target mediators identified in the investigator's prior dynamic modeling study of Gulf War Illness (GWI). The investigator will repeat the dynamic modeling before treatment and on therapy to assess the modeling and the impact of the interventions on the homeostatic networks that have identified, with an added focus on the glutathione/redox system.

Detailed description

In the Investigator's prior study Dynamic Modeling in GWI, the investigator used an exercise stress model (rest, peak oxygen consumption oxygen uptake, and 7 follow-up sampling points) to measure the mediators of relapse in the context of their interactive homeostatic networks. The investigator surveyed the response of genes and blood-borne biomarkers in order to interrogate and map regulation of neuro-endocrine-autonomic-immune function in these subjects as compared to GW era sedentary healthy controls. The investigator's research team applied an integrative systems-based approach rooted in computational biology connecting gene expression and biomarkers to pathways and to symptoms in order to identify potential therapeutic targets as well as optimal strategies for manipulation of these targets. Using this data the investigator's research team has developed a virtual model of the illness, which has been used to identify potential therapeutic targets.

Interventions

DRUGCurcumin

Perform a randomized phase I/II study comparing curcumin (increased bioavailable form, body cell mass-85, 400 mg twice a day) to glutathione (liposomal bioavailable form 630 mg bid), with a 3 month intervention and assessment of safety, efficacy and biomarker response to therapy.

DRUGGlutathione

Perform dynamic modeling studies before and after 3 months of therapy, repeating the method used previously in order to compare the response to exercise across groups and better quantify the degree of recovery in treated subjects using an exercise challenge and 9 point in time blood and saliva collections over 24 hours with genomic, cytokine, neuropeptide and cell population studies.

OTHERPlacebo

Placebo liquid 120 ml per/ bottle Placebo capsules 60 capsules per bottle 400 mg /cap With the addition of a Partner PI, redox/methylation expert Dr. Richard Deth, perform studies of antioxidant and methylation-related metabolic status prior to, during and after acute exercise in GWI subjects before and after interventions.

Sponsors

South Florida Veterans Affairs Foundation for Research and Education
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
35 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Veterans with Gulf War Illness * 35 to 70 years old * Good health by medical history prior to 1990 * Currently have no exclusionary diagnoses that could reasonably explain the symptoms of their fatiguing illness and their severity

Exclusion criteria

* Major depression with psychotic or melancholic features * Schizophrenia * Bipolar disorder * Delusional disorders * Dementias of any type * History or current alcohol abuse * History or current drug abuse * Current tobacco use * Organ failure * Defined rheumatologic * Inflammatory disorders * HIV * Hepatitis B and C * Primary sleep disorders * Steroids * Immunosuppressives

Design outcomes

Primary

MeasureTime frameDescription
Biomarker response to therapy using cytokine panel12 weeksGoal is that both will prove safe for use in GWI patients
Biomarker response to therapy using a VO2 exercise test12 weeksGoal is that both will prove safe for use in GWI patients

Countries

United States

Contacts

Primary ContactFanny V Collado, RN
fanny.collado@va.gov305-575-7000
Backup ContactElizabeth Balbin
ebalbin@med.miami.edu305-275-5450

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026