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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04586049
Other study ID # 2019-0961
Secondary ID A176000EDUC/KINE
Status Recruiting
Phase
First received
Last updated
Start date May 16, 2023
Est. completion date September 2024

Study information

Verified date September 2023
Source University of Wisconsin, Madison
Contact Jill N Barnes, PhD
Phone 608-262-1654
Email jnbarnes@wisc.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Brain blood flow regulation and autonomic dysfunction will be measured in Veterans with and without Gulf War Illness who served in the Gulf War between 1990 and 1992.


Description:

Gulf War Illness (GWI) is a multi-symptom illness with unknown etiology. GWI is a leading cause of disability in Gulf War Veterans. Cognitive complaints are a common symptom of GWI, which suggests the brain is involved in the development of this condition. As Veterans age, these cognitive complaints may worsen and be compounded by the aging process. GWI may be a condition of "accelerated" brain aging. Therefore, there may be long-term consequences of GWI, and the presence of GWI may increase a person's risk for developing Alzheimer's Disease (AD) or other dementias. In comparison to other brain-related diseases such as stroke, relatively little is known about GWI and how this condition impacts the normal age-related changes in the brain. The research aims are: 1. To determine if Veterans with Gulf War Illness demonstrate abnormal brain blood flow regulation and autonomic dysfunction when compared with Veterans without Gulf War Illness. 2. To determine if brain blood flow and autonomic nervous system variables in Veterans are associated with other markers of brain aging that are relevant to cognitive decline.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 68 Years
Eligibility Inclusion Criteria: - Deployed to the Persian Gulf between 1990-1992 - Body mass <300 lbs - Diagnosis of Gulf War Illness based on CMI/CDC and Kansas definitions or No diagnosis of Gulf War Illness Exclusion Criteria: - Current or lifetime evidence of: Type II diabetes, neurological disease, cancer treatment, rheumatoid arthritis, lupus, bipolar disorder, psychotic disorders, or mood disorders with psychotic features - Current illicit substance use or partial remission for less than 1 year - Taking multiple sedatives or anticonvulsant medications - Currently pregnant - Absolute contraindications to exercise testing - Contraindications to MRI - Other significant medical conditions at investigator's discretion

Study Design


Related Conditions & MeSH terms


Intervention

Device:
MRI
Participants will undergo an MRI scan while participating in a breathing test to measure brain blood flow.
Transcranial Doppler Ultrasound
Participants will undergo a TCD scan while participating in a breathing test to measure brain blood flow.
Other:
Sympathetic Nerve Activity
Participants will undergo sympathetic nerve activity testing while participating in a breathing test.

Locations

Country Name City State
United States University of Wisconsin-Madison Madison Wisconsin

Sponsors (2)

Lead Sponsor Collaborator
University of Wisconsin, Madison United States Department of Defense

Country where clinical trial is conducted

United States, 

References & Publications (51)

Barnes JN, Hart EC, Curry TB, Nicholson WT, Eisenach JH, Wallin BG, Charkoudian N, Joyner MJ. Aging enhances autonomic support of blood pressure in women. Hypertension. 2014 Feb;63(2):303-8. doi: 10.1161/HYPERTENSIONAHA.113.02393. Epub 2013 Dec 9. — View Citation

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Barnes JN, Harvey RE, Miller KB, Jayachandran M, Malterer KR, Lahr BD, Bailey KR, Joyner MJ, Miller VM. Cerebrovascular Reactivity and Vascular Activation in Postmenopausal Women With Histories of Preeclampsia. Hypertension. 2018 Jan;71(1):110-117. doi: 10.1161/HYPERTENSIONAHA.117.10248. Epub 2017 Nov 20. — View Citation

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Haley RW, Spence JS, Carmack PS, Gunst RF, Schucany WR, Petty F, Devous MD Sr, Bonte FJ, Trivedi MH. Abnormal brain response to cholinergic challenge in chronic encephalopathy from the 1991 Gulf War. Psychiatry Res. 2009 Mar 31;171(3):207-20. doi: 10.1016/j.pscychresns.2008.05.004. Epub 2009 Feb 20. — View Citation

Haley RW, Vongpatanasin W, Wolfe GI, Bryan WW, Armitage R, Hoffmann RF, Petty F, Callahan TS, Charuvastra E, Shell WE, Marshall WW, Victor RG. Blunted circadian variation in autonomic regulation of sinus node function in veterans with Gulf War syndrome. Am J Med. 2004 Oct 1;117(7):469-78. doi: 10.1016/j.amjmed.2004.03.041. — View Citation

Hubbard NA, Hutchison JL, Motes MA, Shokri-Kojori E, Bennett IJ, Brigante RM, Haley RW, Rypma B. Central Executive Dysfunction and Deferred Prefrontal Processing in Veterans with Gulf War Illness. Clin Psychol Sci. 2014 May 1;2(3):319-327. doi: 10.1177/2167702613506580. — View Citation

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* Note: There are 51 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Brain blood flow measured using Transcranial Doppler ultrasound Neurovascular control will be investigated by measuring the change in brain blood flow using a transcranial Doppler ultrasound in response to a breathing test. Baseline
Primary Brain blood flow measured using MRI Neurovascular control will be investigated by measuring the change in brain blood flow using an MRI in response to a breathing test. Baseline
Primary Sympathetic nerve activity Neurovascular control will be investigated by measuring the change in sympathetic nerve activity will be measured using microneurography in response to a breathing test. Baseline
See also
  Status Clinical Trial Phase
Completed NCT04133701 - Meal Timing and Blood Pressure N/A