Genetic and molecular-biological study of hereditary coagulopathy

Genetic and molecular-biological study of hereditary coagulopathy - Study of hereditary coagulopathy

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000003446

Enrollment

Registered

2010-07-01

Start date

2010-06-01

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

hereditary coagulopathy

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patinents who are suspected to suffer from hereditary coagulopathy.

Exclusion criteria

Exclusion criteria: Patients who do not agree with genetic analysis.

Design outcomes

Primary

Measure	Time frame
Identification of genetic abnormality and molecular abnormality	—

Countries

Japan

Contacts

Public ContactSeiji Kawano

Kobe University Hospital Department of clinical laboratory

sjkawano@med.kobe-u.ac.jp078-382-5111

Outcome results