Migraine Clinical Trial
Official title:
The Combined Effects of omega3 Fatty Acids and Curcumin Supplementation on Gene Expression and Serum Levels of Some Inflammatory and Endothelial Factors in Migraine Patients
The aim of this study is to determine the effects of omega 3 fatty acid, curcumin and their combination or placebo for 2 months on the gene expression of COX-2, iNOS, TNF-α, IL-1β, IL-6, VCAM-1 and ICAM-1 in the peripheral blood mononuclear cell (PBMC) and serum levels of COX-2, iNOS, TNF-α, IL-1β, IL-6, VCAM-1, ICAM-1 and hsCRP of migraine patients.
The aim of this study is to determine the effects of omega 3 fatty acid, curcumin and their
combination or placebo for 2 months on the gene expression of cyclooxygenase-2 (COX-2),
inducible nitric oxide synthase (iNOS), Tumor necrosis factor-α (TNF-α), interleukin-1β
(IL-1β), interleukin-6 (IL-6), vascular cell adhesion molecule-1 (VCAM-1) and intercellular
adhesion molecule-1 (ICAM-1) in the peripheral blood mononuclear cell (PBMC) and serum
levels of COX-2, iNOS, TNF-α, IL-1β, IL-6, VCAM-1, ICAM-1 and high-sensitivity C-reactive
protein (hsCRP) of migraine patients.
In this randomized, double-blind clinical trial, placebo-controlled study, 80 women and men
with migraine are enrolled from the Iranian Center of Neurological Research. At the start of
study, all participants will sign informed consent and complete a general information form.
24-hour food recall for 3 days will be taken from the patients at the beginning and the end
of the study. Selected samples by using stratified randomization method based on sex, gender
and body mass index (BMI) are classified into 4 groups: 1) receiving omega 3 fatty acid
supplement and curcumin supplement 2) receiving omega 3 fatty acid supplement and curcumin
placebo 3) receiving curcumin supplement and omega 3 fatty acid placebo 4) receiving omega 3
fatty acid placebo and curcumin placebo.
The omega 3 fatty acid supplement group will receive 1200 mg Eicosapentaenoic acid (EPA) and
600 mg Docosahexaenoic acid (DHA) totally 1800 mg daily for 2 months. The curcumin
supplement group will receive 1000 mg curcumin daily for 2 months. The omega 3 fatty acid
placebo group will also receive placebo containing 1800 mg edible paraffin oil and curcumin
placebo group will receive 1000 mg starch powder both similar in terms of color, shape and
size. participants are advised to maintain their diet, level of physical activity and
medication dose during the study. Blood samples will be collected after anthropometric
parameter measuring then target biochemical parameters, gene expression and serum levels and
physical activity will be measured before and after the trial.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Supportive Care
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