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Prophylactic Effect of Memantine on Chronic Migraine Headache

The effectiveness of adding Memantine to Topiramate in the prevention of headache attacks among patients with chronic migraine headaches

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191205045623N1
Enrollment
54
Registered
2019-12-26
Start date
2017-04-20
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Migraine headache. Migraine

Interventions

Intervention 1: Intervention group: Patients in intervention group received Memantine tablet 20 mg daily which reached this level after 4 weeks and they received topiramate tablet 50 mg daily as a bas

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 18 to 65 years old Chronic migraine headache according to International Classification of headache

Exclusion criteria

Exclusion criteria: Pregnancy or breast-feeding Renal or hepatic impairment or known cardiovascular disease History of allergy to memantine and topiramate

Design outcomes

Primary

MeasureTime frame
The severity of migraine headache attacks. Timepoint: This evaluation was performed at the beginning of the study, and the end of first, second, third and fourth months of the study. Method of measurement: Visual Analogue Scale.;The disability level of migraine headache attacks. Timepoint: This evaluation was performed at the beginning of the study, and the end of first, second, third and fourth months of the study. Method of measurement: Migraine Disability Assessment Test Survey (MIDAS).;The frequency of migraine headache attacks. Timepoint: This evaluation was performed at the beginning of the study, and the end of first, second, third and fourth months of the study. Method of measurement: Daily headache diary.;The duration of migraine headache attacks. Timepoint: This evaluation was performed at the beginning of the study, and the end of first, second, third and fourth months of the study. Method of measurement: Daily headache diary.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDavood Kashipazha

Ahvaz University of Medical Sciences

dakashi47@gmail.com+98 61 3374 3012

Outcome results

None listed

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