Skip to content

Investigating the effect of spirulina supplement on women with migraine

Investigating the effect of spirulina supplement (Arthrospira platensis) on inflammatory status, oxidative stress, clinical symptoms, mental health and quality of life of women with migraine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240619062185N1
Enrollment
90
Registered
2024-07-11
Start date
2024-07-01
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

migraine. Migraine

Interventions

Intervention 1: Intervention group: The intervention group consumes 1000 mg of spirulina daily in the form of two 500 mg capsules per day after meals for 2 months. Intervention 2: Control group: Contr

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Women with migraine Patients who agree to participate in the study. Diagnosis of migraine by a neurologist based on ICHD-3 criteria Age 18 to 60 years

Exclusion criteria

Exclusion criteria: History of any allergy, intolerance or adverse drug reaction to the study supplement Pregnancy and breastfeeding History of intestinal bypass Following a special diet in the last 3 months Smoking or alcohol consumption Consumption of nutritional and herbal supplements effective on migraines including Riboflavin, evening primrose, feverfew, magnesium and Coenzyme Q10. Having cardiovascular diseases,diabetes, liver, kidney and thyroid diseases and malignancies and other neurological disorders Anticoagulants such as warfarin Patients with immune system disorders

Design outcomes

Primary

MeasureTime frame
High-sensitivity C-reactive protein (hs-CRP). Timepoint: At baseline and after 2 month. Method of measurement: ELISA.;Total antioxidant capacity. Timepoint: At baseline and after 2 month. Method of measurement: colorimetric.;Malondialdehyde. Timepoint: At baseline and after 2 month. Method of measurement: colorimetric.;Serum lactate. Timepoint: At baseline and after 2 month. Method of measurement: colorimetric.;Nitric oxide. Timepoint: At baseline and after 2 month. Method of measurement: colorimetric.;Migraine severity. Timepoint: At baseline and after 2 month. Method of measurement: VAS (Visual Analogue Scale).;Migraine frequency. Timepoint: At baseline and after 2 month. Method of measurement: Number of migraine attacks per month.;Duration of migraine headache. Timepoint: At baseline and after 2 month. Method of measurement: Average duration of migraine attacks in hours per episode.;Migraine Headache Index Score(MHIS). Timepoint: At baseline and after 2 month. Method of measurement: Headache severity × headache frequency × headache duration.;HIT_6(Headache Impact Test). Timepoint: At baseline and after 2 month. Method of measurement: HIT-6 (Headache Impact Test) questionnaire.;Stress. Timepoint: At baseline and after 2 month. Method of measurement: DASS-21 questionnaire.;Anxiety. Timepoint: At baseline and after 2 month. Method of measurement: DASS-21 questionnaire.;Depression. Timepoint: At baseline and after 2 month. Method of measurement: DASS-21 questionnaire.;Quality of Life. Timepoint: At baseline and after 2 month. Method of measurement: MSQ questionnaire(Migraine-Specific Quality of Life Questionnaire).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Gholamreza Askari

Esfahan University of Medical Sciences

askari@mui.ac.ir+98 31 3792 3060

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026