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Comparison of cinnarizine and topiramate in migraine prophylaxis

Comparison of cinnarizine and topiramate in migraine prophylaxis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201201028323N5
Enrollment
126
Registered
2012-01-10
Start date
2011-10-23
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

Condition 1: Common migraine. Condition 2: Classical migraine. Migraine without aura [common migraine] Migraine with aura [classical migraine]

Interventions

Intervention 1: Cinnarizne tablet 25 mg twice a day orally, for 12 weeks. Intervention 2: Topiramate tablets 25 mg twice a day orally, for 12 weeks.
Treatment - Drugs
Topiramate tablets 25 mg twice a day orally, for 12 weeks

Sponsors

Vice-chancellor for research, Kermanshah University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: more than 4 and less than 10 attacks monthly ; interval between attacks more than 48 hours ; age at the onset of headache less than 50 years ; age 18-65 years ; not being pregnant or breast feeding ; discontinuation of other prophylactic drugs one month prior to the study Exclusion criteria: non-migraine headaches ; overuse of medications in migraine attacks (consumption of NSAID, Ergots or Triptans more than 8 days a month) ; substance and alcohol abuse ; illiteracy of patients and their family (unable to fill diaries)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of headache. Timepoint: in each migraine attack. Method of measurement: patient will record the headache severity in daily notes as VAS (from 1 to 10) & physician registers them every 4 weeks.;Duration of migraine attack. Timepoint: in each migraine attack. Method of measurement: patient records the hours of headache in each attack , physician register them every 4 weeks.;Headache frequency. Timepoint: every 4 week. Method of measurement: According to patients daily notes.;Analgesic use. Timepoint: every 4 week. Method of measurement: According to patients daily notes.

Secondary

MeasureTime frame
Clinical side effects. Timepoint: every 4 weeks. Method of measurement: According to patients daily notes.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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