Research to reveal disease mechanisms and to find therapies for hereditary connective tissue disorders

Elucidation of pathomecanisms and development of therapies for hereditary connective tissue disorders

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-jRCT1030230625

Enrollment

400

Registered

2024-02-08

Start date

2024-02-08

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 connective tissue disorders Ehlers-Danlos syndrome

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who have or who are suspected to have hereditary connective tissue disorders

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

Measure	Time frame
Elucidation of pathomechanisms including causative gene variants	—

Secondary

Measure	Time frame
Validation of clinical characteristics of patients found to have causative gene variants and development of ethiology-based therapies	—

Contacts

Public ContactYamaguchi Tomomi

Shinshu University Hospital

t_yamaguchi@shinshu-u.ac.jp+81-263-37-2618

Outcome results