Ketamine in Veterans With Gulf War Illness

Effects of a Single Dose of Intravenous Ketamine on Symptoms of Gulf War Illness in 1990-1991 Gulf War Veterans

Up to one third of the 700,000 U.S. military veterans of the 1990-91 Gulf War have Gulf War Illness (GWI), a symptom complex characterized by a combination of chronic pain, cognitive impairment, debilitating fatigue, gastrointestinal complications, and other persistent symptoms. Epidemiologic studies of 1990-1991 Gulf War veterans have identified the short but intense combined exposure to insecticides (e.g., organophosphates, DEET, permethrin), pills with anti-nerve gas agent pyridostigmine bromide (PB), and low-level chemical nerve agents as likely candidates of GWI. Animal models have shown that these neurotoxicants could induce neuroinflammation which is marked by enhanced inflammatory cytokines, and activated microglia and astrocytes. Inflammation has been linked to GWI. Secondary effects of neuroinflammation and glia activation could be excessive glutamate-mediated neuronal activation. There is currently no treatment for symptoms of GWI. Ketamine is an N-methyl-D-aspartate receptor (NMDAR) antagonist. Besides blocking activation of NMDARs, a sub-anesthetic dose (0.5 mg/kg over 40 minutes) of ketamine could be an anti-inflammatory agent, and could protect microglia and astrocytes from being activated by inflammatory agents. This low dose of ketamine has also been shown to improve fatigue within 24 hours after a single infusion, and to improve inflammatory pain. This makes ketamine a feasible candidate for the treatment of inflammation-associated symptoms of GWI. This pilot study will examine if GWI is related to NMDAR functioning, testing effects of a single 40-minute intravenous infusion of 0.5 mg/kg of ketamine on GWI symptom severity in 21 veterans of the 1990-1991 Gulf War who meet Kansas case definition criteria of GWI.

Study Overview

• Status: Terminated
• Conditions: Gulf War Syndrome
• Intervention / Treatment: Drug: Ketamine Hydrochloride

Detailed Description

Recruitment for this study starts after protocol approval by the BCM IRB, MEDVAMC R&D, and DoD HRPO. All study procedures are for research only.

Potential subjects will be recruited (i) from the Houston community with advertisements in local papers and social media, and with flyers at BCM and MEDVAMC; (ii) among veterans from the 1990-1991 Gulf War who participated in protocol H-40948 and who consented to be recontacted for future studies; (iii) among veterans from the 1990-1991 Gulf War who voluntarily registered in the Gulf War Registry (GWR) because of concerns of possible Gulf War Illness (GWI). Individuals under category (i) will contact us. Individuals under category (ii) will be contacted by phone or text. Individuals under category (iii) will be contacted by letter and, after a 10-day non-response, by phone. Before sending a letter, names in the GWR will be matched with those in CPRS. If in CRPS, medical information will be reviewed to determine study eligibility; if apparently eligible, the letter will be send. If an individual is not in CPRS, the letter will be send. The letter is uploaded in section S.

For the phone call, after providing verbal consent, veterans who are interested in the study, and who did not participate in protocol H-40948, will undergo an in-depth phone pre-screen to determine eligibility. The phone pre-screen inventories symptoms of Gulf War Illness and military history with the Gulf War Military and Health Questionnaire.

This study consists of 3 phases: screening, infusion of ketamine, telephone follow-up.

For phase 1, eligible subjects will provide a urine sample for drug and pregnancy testing, undergo blood pressure testing, will undergo an EKG, will have to provide a 20 ml (2 tsp) blood sample collected for clinical labs (an additional 10 ml (2 tsp) is optional and will be banked for future research), and will visit with a study physician for a medical examination. Finally, we will go over the Gulf War Military and Health Questionnaire assessed during the phone-screen. Total time of phase 1 is 4 to 5 hours.

If qualified for the study, subjects will be scheduled for phase 2: the administration of a single intravenous infusion of 0.5 mg/kg of ketamine. For phase 2, veterans will need to fast for at least 8 hours before the infusion; they can take their medications as prescribed. At arrival at the study site, subjects have to provide a urine sample for drug and pregnancy testing. We will go over their medical information collected in phase 1 to inventory changes, and they will undergo testing of vital signs. Before the infusion at 10 am, subjects will be asked to fill out Gulf War Military and Health Questionnaire (24 hours symptoms). A baseline of possible side effects is established with the CADSS which assess dissociative states. Finally, EEG is collected from the scalp using 4-minute resting EEG (eyes-open/eyes-closed) and 15-minute passive computer paradigm with auditory 85-dB click trains. The infusion of 0.5 mg/kg ketamine is prepared by the MEDVAMC Research Pharmacy. Ketamine is dissolved in 0.9% saline in a bag of saline with a total volume of 100 mL, and administered with an infusion pump at a constant rate. An anesthesiologist will place an indwelling catheter. We will first collect an 10 ml (2 tsp) sample of blood for pro-inflammatory cytokine. Next, the catheter is used for the infusion, which lasts 40 minutes. The EEG and blood collection is repeated at 35-minutes (the peak of ketamine concentration), and again one and two hours later. Subjects will not be discharged before four hours after the end of the infusion.

For phase 3, as part of the research procedures, subjects will be contacted by telephone or telehealth services at a pre-arranged time of mutual convenience on days 1, 2 and 7 after the infusion to inventory 24-hr symptoms with the Gulf War Military and Health Questionnaire. This procedure lasts about 45 minutes to complete

• Study Type: Interventional
• Enrollment (Actual): 1
• Phase: Early Phase 1

Contacts and Locations

Study Locations

• United States
  • Texas
    • Houston, Texas, United States, 77030
      • Marijn Lijffijt

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Military veterans who served for any period of time in the Gulf War Theater of Operations between August of 1990 and July of 1991.
• Cases must meet Kansas GWI case definition criteria.
• Understand the study as described in the informed consent form, and be able to consent for study participation.

Exclusion Criteria:

• A physical or psychiatric illness explaining GWI case definition symptoms at the discretion of the PI.
• History of seizures.
• History of ECT or deep brain stimulation.
• History of head injury with loss-of-consciousness over 15 minutes or no recollection of events.

• Unstable serious illness at the discretion of the PI or study physician, including:

  • hepatic disease
  • renal disease
  • gastroenterologic disease
  • respiratory disease,
  • cardiovascular disease (including ischemic heart disease)
  • endocrinologic disease
  • neurologic disease
  • immunologic disease
  • hematologic disease.
• Clinically significant EKG or laboratory values at the discretion of the study physician.
• Uncontrolled hypertension (systolic BP >160 mm Hg or diastolic BP >90 mm Hg).
• Family history or own history of schizophrenia or psychosis.

• For at least two weeks before ketamine infusion, use of:

  • Antibiotics
  • Antiviral medication
  • anti-inflammatory medications (including NSAIDS) for at least two weeks before ketamine infusion.
• Being pregnant or breastfeeding.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Ketamine; 40 minutes intravenous infusion of 0.5 mg/kg ketamine.	Drug: Ketamine Hydrochloride; Patients with a diagnosis of Gulf War Illness using Kansas Criteria will be enrolled to receive a single 40 minute infusion of 0.5 mg/kg ketamine.; Other Names: Ketelar

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in 40Hz Auditory steady state response (ASSR) EEG power	The 40Hz ASSR is an electrophysiology (EEG) paradigm that presents 1-sec trains of 1-ms 85dB clicks presented at 40Hz. Outcome measure is mean power across 32 - 42Hz averaged across fronto-central electrodes that are attached in a 64-channel electrode cap that is based on a 10-10 distribution.	pre-treatment baseline, 35 minutes after start of infusion (close to ketamine peak) and 95 minutes after start of infusion

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Gulf War Military and Health Questionnaire	Questionnaire developed to screen for cognitive, pain, fatigue and other Gulf War Illness symptoms. Due to its complexity, and variability, no single measure of severity addresses all possible presentations of Gulf War Illness (GWI). Therefore, we used the symptom portion of the Gulf War Military and Health Questionnaire to assess fatigue/sleep problems, somatic pain, skin abnormalities, gastrointestinal, respiratory, and neurologic/cognitive/mood symptoms, based on the Kansas GWI and CDC CMI case definitions. To assess change in current symptoms, participants are asked about the absence (0), presence, and severity (1=mild; 2=moderate; 3=severe) of the symptoms over the past 24 hours. Score range: 0-87; higher scores indicate more and/or more severe symptoms.	pre-treatment baseline and days 1, 2 and 7 after the infusion
Change in 4 minutes resting state EEG	Patients will lay quietly with eyes open for 2 minutes and eyes closed for 2 minutes to extract power of the gamma (40Hz) EEG band.Outcome measure is relative mean EEG power across 31 - 55Hz across fronto-central electrodes attached in a 64-channel electrode cap that is based on a 10-10 distribution.	pre-treatment baseline, 35 minutes after start of infusion (close to ketamine peak) and 95 minutes after start of infusion
Change in CADSS dissociative states scale	The CADSS measures dissociation and psychosis-like experiences that are sometimes experienced acutely with ketamine. The CADSS has 23 clinician-administered items, each scored from 0 (not at all) to 4 (extreme). Minimal score is 0; maximum score is 92. Higher score indicate more severe dissociation and psychosis-like experiences.	Pre-treatment baseline, and 1 hour, 2 hours and 4 hours after start of infusion

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Inflammatory cytokines and metabolites of ketamine in 10 mL blood sample: Exploratory	This sample will be used for future study to examine acute effects of ketamine on inflammatory cytokines and metabolites of ketamine	Pre-treatment baseline, and 1 hour, 2 hours and 4 hours after start of infusion

Collaborators and Investigators

• Sponsor: Baylor College of Medicine
• Collaborators: Michael E. DeBakey VA Medical Center
• Investigators: Principal Investigator: Marijn Lijffijt, PhD, Baylor College of Medicine

Study record dates

Study Major Dates

• Study Start (Actual): February 1, 2021
• Primary Completion (Actual): February 16, 2022
• Study Completion (Actual): February 16, 2022

Study Registration Dates

• First Submitted: November 12, 2020
• First Submitted That Met QC Criteria: January 14, 2021
• First Posted (Actual): January 15, 2021

Study Record Updates

• Last Update Posted (Actual): March 3, 2022
• Last Update Submitted That Met QC Criteria: February 16, 2022
• Last Verified: February 1, 2022

More Information

Terms related to this study

• Keywords: Inflammation; Gulf War Illness; ketamine; N-methyl-D-aspartate
• Additional Relevant MeSH Terms: Occupational Diseases; Persian Gulf Syndrome; Physiological Effects of Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Central Nervous System Depressants; Peripheral Nervous System Agents; Analgesics; Sensory System Agents; Anesthetics, Dissociative; Anesthetics, Intravenous; Anesthetics, General; Anesthetics; Excitatory Amino Acid Antagonists; Excitatory Amino Acid Agents; Ketamine
• Other Study ID Numbers: H-46289

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No
• IPD Plan Description: We have not decided yet what the best way is to share the data. The data will become available, though.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No