Analysis of molecular pathology on diseases that cause retinal degeneration and retinal dysfunction

Analysis of molecular pathology on diseases that cause retinal degeneration and retinal dysfunction - Molecular pathology analysis of retinal dysfunction

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000044906

Enrollment

5000

Registered

2021-07-19

Start date

2021-03-10

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 ContactKosuke Fujita

Nagoya University Graduate School of Medicine Department of Ophthalmology

fujita-k@med.nagoya-u.ac.jp052-744-2275

Outcome results