Skip to content

The effect of an anti-inflammatory diet on severity, frequency, duration of headache, IL-6 level and anthropometry in patients with migraine

The effect of an anti-inflammatory diet on severity, frequency, duration of headache, IL-6 level and anthropometry in patients with migraine

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170929036477N5
Enrollment
60
Registered
2021-08-14
Start date
2021-08-11
Completion date
Unknown
Last updated
2021-08-30

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: 25 Migraine patients follow a three-month anti-inflammatory diet(includes daily intake of fruits and fresh vegetables (raw or cooked in various colors), whole grain

Sponsors

Shahre-kord University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Willingness to cooperate with the plan Diagnosis of migraine by a neurologist based on ICHD-3 criteria. Age 20 to 50 years. No chronic diseases (liver, kidney, cardiovascular disease, secondary headache or other types of primary headache except migraine) Absence during pregnancy and lactation .. Taking dietary supplements or medication (nutritional supplements, multivitamin mineral and W3 supplements or anti-migraine medications (valproate, amitriptyline, etc.), anti-inflammatory and anti-depressant pills, Aspirin and NSAIDs, contraceptives in the last three months Failure to follow a specific diet or exercise program during the last three months No alcohol and smoking

Exclusion criteria

Exclusion criteria: Failure to follow the recommendations and diet. Failure to refer the person at different stages of the study. Cardiovascular disease, hypertension, diabetes, liver, kidney, thyroid, malignancies and other neurological disorders. Taking nutritional and herbal supplements that affect migraines including riboflavin, feverfew, magnesium and coenzyme Q10

Design outcomes

Primary

MeasureTime frame
Severity of migraine. Timepoint: At the beginning of the study (before the intervention) and three months after the start of adherence to die. Method of measurement: Visual Analogue Scale.;Migraine frequency. Timepoint: At the beginning of the study (before the intervention) and three months after the start of adherence to die. Method of measurement: Question / Number of attacks per month.;Duration of migraine headache. Timepoint: At the beginning of the study (before the intervention) and three months after the start of adherence to die. Method of measurement: Question / Average duration of each migraine attack.;The degree of disability caused by migraines. Timepoint: At the beginning of the study (before the intervention) and three months after the start of adherence to die. Method of measurement: Headache Impact Test Questionnaire.;IL-6. Timepoint: At the beginning of the study (before the intervention) and three months after the start of adherence to die. Method of measurement: Kit Eliza.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSiavash fazelian

Shahre-kord University of Medical Sciences

siavashfazelian@yahoo.com+98 912 839 0366

Outcome results

None listed

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