Novel Immune Markers in Patients With Multiple Sclerosis
NCT ID: NCT01026272
Last Updated: 2010-07-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
120 participants
OBSERVATIONAL
2010-01-31
2011-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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healthy subjects
subjects with no sign of inflammatory disease, or diagnosis of MS
No interventions assigned to this group
Patients with MS
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Not currently in "relapse" or exacerbation.
3. Age \> 21 and \< 50.
4. Subjects must be able to attend study visits at screening, baseline and time points of 4, 12 and 24 weeks.
5. Diet, exercise, and supplementation must be kept constant throughout participation in the study.
6. Ability to read and speak English.
1. Current.
2. Age \> 21 and \< 50.
3. Subjects must be able to attend study visits at screening, baseline and time points 4, 12 and 24 weeks.
4. Diet, exercise, and supplementation must be kept constant throughout participation in the study.
5. Ability to read and speak English.
Exclusion Criteria
2. Diagnosis of any bleeding disorder (hemophilia, vonWillebrands, menorrhagia, hypercoaguability, history of clots, thrombocytopenia). Any patient with one of these diagnoses and/or any patient on any of/combination of the following medications would not be eligible for participation: ANTICOAGULANT/ANTIPLATELET DRUGS: Some of these drugs include aspirin, clopidogrel (Plavix), dalteparin (Fragmin), dipyridamole (Persantine), enoxaparin (Lovenox), heparin, ticlopidine (Ticlid), warfarin (Coumadin).
3. Hormone Replacement Therapy or oral contraception pills or pregnancy.
4. Use of clinical Cannabis for MS symptom control or recreationally in the last 6 months.
5. Previous diagnosis of DSMV criteria.
6. Use of tobacco, either orally or inhaled.
7. BMI \>27 or \<19.
8. Diagnosis of Diabetes (fasting blood sugar over 125 mg/dl).
9. Performance athletes.
10. Medical history/diagnosis of autoimmune or other chronic inflammatory disease or serious immunologically-related health condition.
11. Lactose intolerance (in-ability to eat/drink milk products without problems).
12. Allergy to fish or seafood. Theoretically, some people who are allergic to seafood such as fish might also be allergic to fish oil supplements. There is no reliable information showing how likely people with seafood allergy are to have an allergic reaction to fish oils; however, until more is known advise patients allergic to seafood to avoid or use fish oil supplements cautiously.
13. High dose supplement/botanical therapy which may have an effect on bleeding times: Vitamin E (greater than 400 IU/qd); adn/or daily use of any/combination of the following botanical therapy: Angelica sinensis; Allium sativum; Zingiber officinale; Ginkgo biloba; and Salix alba.
21 Years
50 Years
ALL
Yes
Sponsors
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University of Washington
OTHER
Responsible Party
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University of Washington
Principal Investigators
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Michelle Sexton, ND
Role: PRINCIPAL_INVESTIGATOR
University of Washington
Locations
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University of Washington
Seattle, Washington, United States
University of Washington
Seattle, Washington, United States
Countries
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Facility Contacts
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Other Identifiers
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A50879
Identifier Type: OTHER
Identifier Source: secondary_id
35083-B
Identifier Type: -
Identifier Source: org_study_id
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