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临床试验/NCT02206490
NCT02206490已完成2 期

Trial of Naltrexone and Dextromethorphan for Gulf War Veterans Illnesses

East Carolina University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2012年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Symptoms Scores

研究概览

简要总结

Veterans of the 1991 Gulf War who developed Gulf War Illness are being studied. Treatments with FDA approved generic drugs are being administered to see if they help with the symptoms of Gulf War Illness, such as chronic fatigue; difficulty with memory, concentration, and thinking; widespread chronic pain; and autonimic dysfunction. Drugs to be tested are dextromethorphan and naltrexone.

详细描述

Gulf war veterans' illnesses comprise distinct clusters of symptom-defined illnesses for which there are neither diagnostic tests nor effective treatments. Gulf war veterans had variable exposures to a number of chemicals, including organophosphate insecticides, pyrethrum-related insecticides, DEET, Pyridostigmine bromide, smoke from oil well fires, and Sarin gas. Gulf war veterans' illnesses may reflect an inflammatory cycle involving the brain which may be a common mechanism of many neurological conditions, whether initiated by toxic exposures, infection, or trauma. In this theory, central nervous system inflammation initiated by toxic exposures and sometimes exacerbated by subsequent exposures is a component of illness hypothesized to explain the neurological manifestations. Substance P release at sensory nerve endings is an explanation for the peripheral pain manifestations of illness.

This theory suggests that novel anti-inflammatory drugs may be of benefit in symptom-defined illnesses related to a cycle of inflammation. Dr. J. S. Hong's laboratory at the National Institute of Environmental Health Sciences has demonstrated that Morphine-related analogs, including Naltrexone and Dextromethorphan, have great potency in anti-inflammation and neuroprotective effects. Naltrexone is a safe and readily available generic medication. Dextromethorphan is also a safe and readily available generic medication that is available without a prescription as a cough medication. Results from several clinical trials showed that Naltrexone is effective in several inflammation-related diseases, such as neurogenic pain, movement disorders, etc. In addition, there were no obvious side effects in patients taking this drug for six months. This project will conduct randomized double-blinded studies for treating ill Gulf war veterans with Naltrexone and Dextromethorphan. Laboratory tests for markers of inflammation including neurogenic inflammation will be performed pre- and post-treatment, to see if these markers are elevated and if so, to see if treatment modulates these markers.

Ill Gulf veterans will be recruited through the media, veterans groups, and individual veteran activists. A screening telephone interview will be performed to determine if the veterans meet a modified Kansas case definition for inclusion. Those veterans who meet study criteria will be invited to participate. Eligible veterans will be invited for an initial visit that will consist of obtaining written informed consent, a medical history, physical examination, and laboratory testing. Institutional review board approval of the study will be in place. The pharmacy staff at the institution will prepare the medications and placebo in identical capsules.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Served in the Gulf War and developed the symptoms of Gulf War Illness as described by the modified Kansas Case Definition

排除标准

  • Pregnant women, nursing mothers, individuals requiring medications that have drug interactions with dextromethorphan or naltrexone, cancer not in remission, chronic infectious disease, liver disease, lupus, multiple sclerosis, stroke, under current treatment for schizophrenia, bipolar disorder/manic depression, and depression.
  • Those with a history of current illicit drug use will be excluded. Individuals who have had recent surgery will not be enrolled until they have completely recovered from the surgery.
  • Subjects participating in other clinical trials will be excluded.
  • Those enrolled recently in a clinical trial will be enrolled after a washout period of one month.

研究组 & 干预措施

Naltrexone Study Drug

Active Comparator

Subjects will take naltrexone 4.5 mg daily for three months.

干预措施: naltrexone (Drug)

Naltrexone placebo

Placebo Comparator

Subjects will take a 3 month course of a placebo pill identical in appearance to the naltrexone study drug.

干预措施: naltrexone (Drug)

dextromethrophan study drug

Active Comparator

subjects will take a sustained release dextromethorphan pill twice a day.

干预措施: Dextromethorphan (Drug)

dextromethoprhan placebo

Placebo Comparator

Subjects will take a 3 month course of a placebo pill identical in appearance to the dextromethorphan study drug.

干预措施: Dextromethorphan (Drug)

结局指标

主要结局

Symptoms Scores

时间窗: 28 weeks approximately

Symptoms of Gulf War Illness will be scored by participants using a ten center meter scale. Scores will be collected at the end of 12 weeks/16 weeks/28weeks

次要结局

  • Connors Continuous Performance Test(28 weeks approximately)
  • SF-36(28 weeks approximately)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

William J. Meggs

Professor

East Carolina University

研究点 (1)

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