View Clinical Trial (Medical Research Study)
Sleep Disordered Breathing in Gulf War Syndrome Veterans and the Effect of Continuous Positive Airway Pressure (CPAP) Treatment - NCT00252629-11768(Clinical Trial 133155)
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| City: |
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Northport |
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State:
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NY |
| Zip Code: |
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11768 |
| Conditions: |
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Apnea, Sleep - Chronic Fatigue Syndrome |
| Purpose: |
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The purpose of this study is to determine any sleep disordered breathing in veterans with
Gulf War Syndrome (GWS) and compare it to healthy normal asymptomatic Gulf War veterans.
This study will also determine the effect of treatment with continuous positive airway
pressure on veterans with Gulf War Syndrome.
1. The investigators hypothesize that sleep complaints (insomnia, un-refreshing sleep and
daytime fatigue) among GWS patients are related to increased sleep fragmentation in GWS
patients.
2. The investigators hypothesize that increased collapsibility of the upper airway during
sleep with the development of inspiratory flow limitation (IFL) causes the increased
sleep fragmentation in GWS patients.
3. The investigators hypothesize that correction of IFL in GWS patients will result in an
improvement of their sleep quality resulting in an improvement of their sleep
complaints and other functional symptoms.
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| Study summary: |
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Hypothesis 1: To demonstrate that compared to Gulf War Veterans without GWS, GWS patients
have decreased total sleep and increased sleep fragmentation
In order to accomplish this goal and subsequent goals, we will assemble two samples of Gulf
War veterans. The first will be a sample of male GWS patients and the second will be a
sample of male Gulf War veterans without GWS (Gulf War veteran control group). All of the
GWS patients will be registered in the Gulf War Veterans Registry. To avoid referral bias
favoring the presence of IFL during sleep, we will enroll GWS patients by contacting them
from the Registry and inviting them to participate. Gulf War veteran controls will be
recruited in the same way and by advertisement. Prospective study participants will be
screened on several self-report instruments to determine eligibility and assignment to the
GWS group or to the Gulf War veteran control group. Criteria for assignment to the GWS group
are scores above the designated clinical cutpoint on each of three instruments measuring
cognitive difficulties, pain, and fatigue. Conversely, criteria for assignment to the GW
Veteran control group will require scores in the non-clinical range on each of those
instruments. Every subject will have a full night polysomnogram.
Hypothesis 2: To demonstrate that the presence of IFL during sleep among GWS patients
distinguishes them from Gulf War veterans without GWS
A second sleep study will be used to accomplish this second objective. Using precise
methods, we will quantify the prevalence of IFL during sleep in GWS patients and in Gulf War
veteran controls. Following completion, each study will be staged using Rechtschaffen and
Kales criteria. From each study, 3 three minute periods of continuous NREM sleep (a total of
approximately 120 breaths) will be randomly selected and analyzed for the prevalence of flow
limited breaths. During the three minute periods, all of the breaths will be analyzed
whether they occur during sleep or during brief (< 15 second) arousals.
Hypothesis 3: To demonstrate that relief of IFL during sleep will result in improvement of
the functional symptoms of GWS patients
We will accomplish this utilizing a double blind, placebo-controlled trial of nasal
continuous positive airway pressure (CPAP) in GWS patients. Functional symptoms will be
assessed using validated, self-report questionnaires and daily ratings of symptoms with an
electronic diary. |
| Criteria: |
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Inclusion Criteria:
- First Gulf War veterans with and without the syndrome
- Males
- Between 32 and 52 years of age
- No history of current alcoholism nor opiate use
- No history of current active depression nor post-traumatic stress disorder (PTSD)
Exclusion Criteria:
- Females
- History of active alcoholism or opiate drug use
- History of active depression and PTSD |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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July 21, 2010 |
Modifications to
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