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Gliatamine for the migraineurs with cognitive complaint

Efficacy and safety of Gliatamine for the migraineurs with cognitive complaint: A pilot study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0004659
Enrollment
43
Registered
2020-01-28
Start date
2019-04-15
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

None listed

Interventions

Drug : Gliatamine 400mg 2t qd for 12weeks

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with migraine headaches in need of prophylaxis who meet all of the following criteria may participate in this clinical trial. 1. Whom agrees to participate in the study 2. Adults 19 – 85 years old 3. Those who meet the ICHD-III beta migraine diagnostic criteria and complain of cognitive decline * Those who complain of cognitive decline Are not dementia due to mild cognitive impairment (MCI) and have an MMSE of 22 to 26 or less -Patients with “subjective memory disorder” complain of memory disorder even though normal on cognitive function test and not mild cognitive impairment or dementia 4. Who can read and understand the questionnaire? 5. For women of childbearing age who are taking appropriate contraception or who are negative on a pregnancy test.

Exclusion criteria

Exclusion criteria: 1. Subjects suspected of having drug withdrawal due to headache seizures during baseline or evaluation 2. First-time migraine sufferers at age 50 or older. 3. Subjects with advanced neurological disease 4. Subjects with renal or hepatic insufficiency (patients whose blood creatinine, AST, ALT, and total bilirubin levels are at least 1.5 times the upper limit of normal) 5. Subjects with severe cardiovascular disease 6. Subjects with hypersensitivity to glycatamine 7. Pregnant and lactating women 8. Subjects who participate in other clinical trials under research and development 9. If the researcher judges that participation in this study poses a threat to the well-being of the subject or results in an unreliable evaluation at the end of the study. 10. Subjects with a history of peptic ulcer 11. Subjects with a history of allergies to NSAIDs 12. Subjects who received migraine prophylaxis within the last 4 weeks (including propranolol, sibelium, verapamil, tricyclic antidepressant, valproic acid, topiramate, gabapentin) 13. Subjects with a history of alcohol and drug abuse.

Design outcomes

Primary

MeasureTime frame
Korean-Mini-Mental State Examination (K-MMSE)

Secondary

MeasureTime frame
MIDAS (Migraine Disability Assessment)

Countries

Korea, Republic of

Contacts

Public ContactWoo-Jin Lee

Seoul National University Hospital

Outcome results

None listed

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