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Study of the effecacy of CO Q10 in the prophylactic tretment of migraine

Study of the efficacy of CO Q10 in the prophylactic treatment of patient with migraine headache

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014083118992N1
Enrollment
80
Registered
2015-01-29
Start date
2014-09-12
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

migraine. Migraine without aura [common migraine]Migraine with aura [classical migraine]

Interventions

Intervention 1: control group will receive common treatment for migraine prophylaxis. Intervention 2: intervention group will use CoQ10 for six months in addition to their traditional medicines. COQ10
Treatment - Drugs
control group will receive common treatment for migraine prophylaxis
intervention group will use CoQ10 for six months in addition to their traditional medicines. COQ10 will prescribe with a dose of 100 mg per day orally

Sponsors

Research Department of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: inclusion criteria: A definitive diagnosis of migraine based on IHS criteria; having at least one headache per week or 4 per month or having less frequent attacks providing that there is another indication for prophylactic treatment such as suffering from long-lasting disabling attacks; signing informed consent forms by the patient .Exclusion criteria: Having another serious disease such as diabetes, hypertension, thyroid disease, or asthma that interferes with migraine or its preventive treatment; using COQ10 during the last month before study involvement by the patient for another reason; consuming drugs with potential effects of aggravating migraine attacks such as OCP, nitrate compounds, vasodilatators, ...; failure to follow-up the patient for 6 months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache. Timepoint: 1,3,6 months. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Associated symptoms of Migraine. Timepoint: 1.3.6 month. Method of measurement: Questionnaires and Interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Mohsen Soltani

Mashhad University of Medical Sciences

soltanism901@mums.ac.ir+98 51 3840 0000

Outcome results

None listed

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