Gulf War Illness Inflammation Reduction Trial

Completed · Phase 2 · Has a placebo group

Conditions studied: Chronic Inflammation, Chronic Pain, Fatigue, Cognitive Impairment

In brief

The primary objective of this clinical trial is to determine if treatment with an anti-inflammatory drug (delayed-release prednisone) improves the health-related quality of life (HRQOL) of veterans with Gulf War Illness (GWI). The primary outcome measure is a change from baseline of HRQOL with respect to physical functioning and symptoms. Secondary outcomes measures include changes from baseline levels of GWI-associated biomarkers of inflammation in peripheral blood, GWI-associated symptoms (chronic pain, fatigue, and cognitive impairment), and HRQOL with respect to mental functioning.

Key facts

Study ID

NCT02506192

Run by

Minneapolis Veterans Affairs Medical Center

People needed

83

Starts

2015-07-01

Expected to finish

2023-10-19

Last updated by the study team

2024-12-10

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Scores moderate-severe on at least 3 out of 6 domains from the Kansas GWI Case Definition
• Deployed, (and honorably discharged), from the Kuwaiti Theater of Operation (August 2, 1990-July 31, 1991)

You may not qualify if…

• Hospitalization anytime since 1990 for Alcohol or Drug Dependence, Depression, or PTSD
• Known hypersensitivity to Prednisone
• Liver, (active or recent Hepatitis B or C treatment with a completion date within the past 6 months, or alcohol liver disease), or Kidney Disease (Hep B and C ok if after 6 months of treatment)
• Treated Diabetes
• Females who are Pregnant or Nursing
• Female who refuses to use an accepted method of birth control
• Exclusionary Labs: C-Reactive Protein >25, Creatinine Clearance <30, EFGR ≥ 30, Hgb A1-C >7, Glucose >120, WBC >12, RBC >6.2, Hematocrit >60, Hemoglobin <11, Platelets <100, Liver Function Tests (2 x the upper limit of AST and ALT, 2 x the upper limit of Total Bilirubin, and Alkaline Phosphatase)
• Has Inflammatory Arthritis (RA, or Psoriatic Arthritis, Spondylitis, Polyarthritis)
• Reactive Arthritis, or IBD associated Arthritis
• Has any major inflammatory disease (acute Chronic Infections, Ulcerative Colitis, Crohn's Disease, Inflammatory lung diseases- COPD or Asthma requiring steroid treatment, Pericarditis, Vasculitis)
• Has an chronic/active infection
• Chronic use of Prednisone or Corticosteroids (occasional inhaled use of steroids acceptable)
• Active Gum Disease or Dental Infection
• Has been diagnosed with Lupus, Stroke, or Multiple Sclerosis. or any other diagnosis that produces symptoms of fatigue, cognitive impairment, or pain will be excluded based on the Kansas GWI Case definition
• Has a condition that may interfere with the ability to accurately report symptoms, (Severe Psychiatric Problems, Schizophrenia, Bipolar Disorder, Alcohol or Drug Dependence requiring hospitalization, or regular illegal drug use)
• Heart Disease (other than Hypertension), Heart Failure or Coronary Heart Disease requiring hospitalization within the past 12 months
• Cancer (other than basal cell skin cancer), requiring treatment within the past 12 months, or life expectancy of less than 1 year.
• Hospitalization within the past 3 months

Where it is running

• Minneapolis Veterans Affairs Medical Center — Minneapolis, Minnesota, United States

Full record on ClinicalTrials.gov

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