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Comparison of the efficacy of topiramate and sodium valporate in migraine headaches

Comparison of the efficacy of low dose topiramate and sodium valporate in migraine prophylaxis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201011025076N1
Enrollment
80
Registered
2011-03-01
Start date
2009-05-22
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

Classic migraine. Classic(with aura)migraine

Interventions

Intervention 1: Topiramate tablet(25 mg)twice a day orally for 12 weeks. Intervention 2: Sodium valproate tablet(200 mg)twice a day orally for 12 weeks.
Treatment - Drugs
Topiramate tablet(25 mg)twice a day orally for 12 weeks
Sodium valproate tablet(200 mg)twice a day orally for 12 weeks

Sponsors

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

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patient’s age between 20 and 45 years, discontinuation of other prophylactic drugs one month prior to study, interval between attacks more than 48 hours Exclusion criteria: pregnancy and breast feeding, non-migraine headaches, overuse of medications in migraine attacks (consumption of NSAID, Ergots & Triptans more than 8 days a month), substance and alcohol abuse, illiteracy of patients and their family (unable to fill diaries) minimal age:20 maximal age:45 sex:female

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache severity. Timepoint: On each episode of headache. Method of measurement: The patient registers the severity of her headaches in daily notes according to VAS(FROM 1 TO 10)and these notes are registered by physician monthly.;Headache duration. Timepoint: On each headache episode. Method of measurement: The patient registers the duration of each headache episode and these data are registered by the physician monthly.;Headaches frequencies. Timepoint: Monthly. Method of measurement: According to patient's notes.;Analgesic consumption rate. Timepoint: Monthly. Method of measurement: According to patient's notes.

Secondary

MeasureTime frame
Clinical side effects. Timepoint: Every 4 weeks. Method of measurement: According to patients daily notes.;Blood cell count & liver function test changes. Timepoint: Before and at the end of treatment course. Method of measurement: Lab tests.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Alireza Yarahmadi

Ahvaz Golestan Hospital

Yarahmadi_md@yahoo.com; Yarahmadi_md@ajums.ac.ir+98 61 1320 9024

Outcome results

None listed

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