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Analysis of inflammatory cells, soluble factors, molecules as mediators of retinal neural dysfunction and death

Analysis of inflammatory cells, soluble factors, molecules as mediators of retinal neural dysfunction and death - Analysis of molecular mechanisms of retinal neural dysfunction

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000019837
Enrollment
260
Registered
2015-11-18
Start date
2014-05-26
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 dysfunction, retinal degeneration

Interventions

None listed

Sponsors

Tohoku University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Retinal degenration with little pigmentation or atypical Retinal degeneration or retinal degeneration with causative mutations unidentified. Intraocular inflammation. Patient strongly suspected of having reduced vision, signs of retinal structual or electrophysiological abnormalities.

Exclusion criteria

Exclusion criteria: patients that were judged to be inappropriated by the physician. Intraocular surgery within 2 weeks.

Design outcomes

Primary

MeasureTime frame
Whether one can replicate the pathology in mice using patient's serum.

Secondary

MeasureTime frame
Identification of autoantigen for autoimmune retinopathy

Countries

Japan

Contacts

Public ContactKOJI Nishiguchi

Tohoku University Graduate School of Medicine Department of Advanced Ophthalmic Medicine

nishiguchi@oph.med.tohoku.ac.jp+81-22-717-7294

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026