Evaluation of Coagulation in Multiple Sclerosis



Status:Completed
Conditions:Neurology, Multiple Sclerosis
Therapuetic Areas:Neurology, Other
Healthy:No
Age Range:18 - Any
Updated:7/29/2017
Start Date:October 2012
End Date:May 2016

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A Cross-Sectional Study of Coagulation in Multiple Sclerosis

Recent research in multiple sclerosis (MS) have suggested that altered coagulation and
vascular inflammation may play a role in pathophysiology of MS. Sonoclot is viscoelastic
method of analyzing clot formation. This instrument will be used to compare coagulation in
individuals with MS to healthy controls. A 24-hour dietary recall and food frequency
questionnaire will help determine whether coagulation is modified by fish consumption.

This case-control study will recruit individuals with a diagnosis of MS and healthy controls.
Individuals will be asked to come to Bastyr Clinical Research Center for a single study
visit, at which time dietary intake, current medications and supplements, other medical
diagnoses, and coagulation will be evaluated.

Inclusion Criteria:

- Diagnosis of clinically probable of clinically definite multiple sclerosis made by
board certified neurologist. Subject must be willing to release medical information
regarding diagnosis

- Controls must consider themselves healthy and be free of any neurological, autoimmune,
endocrine or other chronic disease. Must also be free of any recent acute
illness/injury that can influence inflammatory activity.

- Individuals must be 18 or older

Exclusion Criteria:

- Diagnosis of coagulation defect

- Use of anticoagulants (eg. warfarin, coumadin) or Aspirin within 30 days of entry.

- NSAID within 7 days of entry (dietary intake of fish oil or tumeric is acceptable)

- Pregnancy
We found this trial at
1
site
Kenmore, Washington 98028
Principal Investigator: Laurie K Mischley, ND
Phone: 425-602-3306
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mi
from
Kenmore, WA
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