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Research on Headache Diagnosis Performance by Headache Diagnosis Program

Research on Headache Diagnosis Performance by Headache Diagnosis Program - HM103-01

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1030240662
Enrollment
Unknown
Registered
2025-02-05
Start date
2024-12-09
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Primary headache or suspected primary headache primary headache

Interventions

None listed

Sponsors

Kawata Yumi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Men and women 18 years of age or older 2)Patients are able to obtain written consent for participation in this study of their own free will using the explanation and consent documents approved by the ethics review committee of each research institution. 3) Patients who come to the hospital for the first time with headache as the main complaint (including referrals from other hospitals). 4) Patient has been diagnosed with primary headache or suspected primary headache (one of the following) by a headache specialist at the initial visit. Migraine or substance abuse headache (MOH) (ICHD-3 code 1 or 8.2) Tension-type headache (ICHD-3 code 2) Trigeminal or autonomic headache (ICHD-3 code 3) Other primary headache (ICHD-3 code 4) Other than primary headache (ICHD-3 code other than above) 5) All the information in the medical questionnaire and the medical record are all tied to each other and there are no missing observation items.

Exclusion criteria

Exclusion criteria: 1) Is currently participating in an interventional study (including clinical trials) other than this study. 2) The patient has a diagnosis of urgent secondary headache. 3) The patient has unclear or other unreadable entries in the records, including neurological findings, in the medical questionnaire or medical record. 4) Other information deemed inappropriate by the principal investigator as the subject of the information.

Contacts

Public ContactYumi Kawata

Clinical Development

yumi.kawata@h-medtech.com+81-90-7554-8471

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026