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Burden of Illness Study among Patients with Narcolepsy or Idiopathic Hypersomnia in Japan

Burden of Illness Study among Patients with Narcolepsy or Idiopathic Hypersomnia in Japan - Burden of Illness Study among Patients with Narcolepsy or Idiopathic Hypersomnia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000059563
Enrollment
300
Registered
2025-11-01
Start date
2025-11-01
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

Narcolepsy, Idiopathic hypersomnia

Interventions

None listed

Sponsors

Takeda Pharmaceutical Company Limited
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Having a self-reported diagnosis of narcolepsy or IH 2. Aged 18 years or older at the time of enrolment into study 3. Can read and understand Japanese 4. Willing to participate in the study and complete the questionnaire, and have accepted the informed consent form

Exclusion criteria

Exclusion criteria: Currently enrolled in any clinical trial

Design outcomes

Primary

MeasureTime frame
Total Cost and Health utilities

Secondary

MeasureTime frame
- Estimate the association between symptoms and costs and health utilities, among patients with NT1, NT2, and IH. - Describe HCRU in relation to disease type and severity measured by JESS, among patients with NT1, NT2, and IH. - Investigate the association of disease severity measured by JESS with education, work status, and work performance, among patients with NT1, NT2, and IH. - Describe the impact of disease severity measured by JESS on ability to operate motor vehicles, among patients with NT1, NT2, and IH.

Countries

Japan

Contacts

Public ContactYu Osada

Takeda Pharmaceutical Company Limited Japan Medical Office

yu.osada@takeda.com03-3278-2111

Outcome results

None listed

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