Skip to content

Effects of levetiracetam, sodium valproate, and nortriptyline on migraine headaches

Comparison of the effects of levetiracetam, sodium valproate, and nortriptyline on migraine headaches control in migraine patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140519017756N39
Enrollment
120
Registered
2018-02-20
Start date
2018-01-30
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Migraine headaches. Migraine

Interventions

Intervention 1: Intervention Group 1 (Levetiracetam): These patients will receive levetiracetam which will start at a dose of 250 milligrams per day in the first week followed by an increased dose of

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Presence of migraine headaches (headache attacks over 3 attacks per month; each attack with an interval of more than 48 hours of relief from other attacks) Age from 18 to 65 years Non-use of other anti-migraine drugs since at least one month ago No allergy to levetiracetam, sodium valproate, and nortriptyline or their compounds Absence of acute migraine resistant to treatment Not having severe mental disorders Absence of neurodegenerative disorders No malignancy Absence of pain disorders No severe infection Informed consent for participation

Exclusion criteria

Exclusion criteria: Pregnant or breast-feeding women Irregular consumption of medications Suffering from severe drug side-effects during the course of the study, which may change treatment regimen Treatment-resistant acute migraine Severe psychiatric disorders Drug or alcohol dependence Renal dysfunction Excessive use of acute migraine drugs

Design outcomes

Primary

MeasureTime frame
Headache severity. Timepoint: At the end of intervention. Method of measurement: Visual analogue scale.;Frequency of headache incidence. Timepoint: After intervention. Method of measurement: Patient daily notes during intervention.;Side effects (digestive, nervous, etc.). Timepoint: After intervention. Method of measurement: Patient daily notes during intervention.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Ahani

Birjand University of Medical Sciences

Zahra_m305@yahoo.com+98 56 3239 5001

Outcome results

None listed

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