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Novel Immune Markers in Patients With Multiple Sclerosis

Quantification of Novel Immune Markers in Human Serum of Patients With MS

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01026272
Acronym
NIMMS
Enrollment
120
Registered
2009-12-04
Start date
2010-01-31
Completion date
2011-05-31
Last updated
2010-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis

Keywords

Endocannabinoid, Fish Oil, Multiple Sclerosis, Monocyte Migration

Brief summary

The investigators hypothesize that the endogenous cannabinoid signalling system has lost homeostasis in the disease multiple sclerosis (MS). To investigate a novel action of dietary fish oils, the investigators will administer a food frequency questionnaire to both healthy subjects and patients with MS. The investigators will first determine if there are differences between both populations of endogenous cannabinoids, and then determine whether dietary intake of fish oils alters these levels

Interventions

None listed

Sponsors

University of Washington
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion Criteria for MS patients: 1. Diagnosis of Multiple Sclerosis (relapsing, remitting) made by a clinical neurologist within the previous 5 years by either MRI (\> 3 white matter lesions) or score of 3-5 on the Kurtzke Expanded Disability Status Scale. 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. Inclusion criteria for healthy subjects: 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

1. Supplementation with fish oils in the last six months. 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.

Design outcomes

Primary

MeasureTime frame
Quantification of endogenous cannabinoidsone time blood draw

Secondary

MeasureTime frame
Monocyte migrationone time blood draw

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026