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Frequency of genetic mutation in Korean Frontotemporal dementia patients

Analysis of Blood and Cerebrospinal Fluids for detecting Genetic mutation, polymorphis and biomarkers in frontotemporal dementia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0000685
Enrollment
100
Registered
2013-02-20
Start date
2012-10-25
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Pusan National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Knopman et al. 2008 research criteria for FTD

Exclusion criteria

Exclusion criteria: Other neurodegenerative dementia

Design outcomes

Primary

MeasureTime frame
genetic mutation (C9orf72)—

Secondary

MeasureTime frame
genetic mutation (MAPT, GRN)—

Countries

Korea, Republic of

Contacts

Public ContactEun Joo Kim

Pusan National University Hospital

Outcome results

None listed

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