Genetic analysis of diseases that cause retinal degeneration/ retinal dysfunction

Genetic analysis of diseases that cause retinal degeneration/ retinal dysfunction - Genetic analysis of retinal dysfunction

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000019624

Enrollment

1000

Registered

2015-11-10

Start date

2014-06-12

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

retinal degeneration, retinal dysfunction

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with retinal degeneration/retinal dysfunction presumably caused by genetic defects

Exclusion criteria

Exclusion criteria: Failed to obtain consent.

Design outcomes

Primary

Measure	Time frame
Identification of pathogenic mutations.	—

Countries

Japan,Europe

Contacts

Public ContactKOJI Nishiguchi

Tohoku University Graduate School of Medicine Department of Ophthalmology

nishiguchi@oph.med.tohoku.ac.jp022-717-7294

Outcome results