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Natural history study of inherited retinal diseases

Natural history study of inherited retinal diseases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117366
Enrollment
Unknown
Registered
2026-01-22
Start date
2023-07-11
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inherited retinal diseases (IRDs)

Interventions

Observational group:None

Sponsors

Renmin Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Clinical phenotype that conforms to a certain hereditary retinopathy; 2.Precursors of hereditary retinopathy in the family line; 3.There is a clear genetic test that suggests hereditary retinopathy;

Exclusion criteria

Exclusion criteria: 1.Various external factors such as trauma and other systemic diseases affect the observers of this study. 2.Unable to cooperate with the inspector;

Design outcomes

Primary

MeasureTime frame
Visual evoked potential;Electrophysiological electroretinogram in ophthalmology;Best corrected visual acuity;Optical coherence tomography;Fundus autofluorescence;Visual field;Color vision test;Panoramic fundus photography;

Countries

China

Contacts

Public ContactYin Shen

Renmin Hospital of Wuhan University

yinshen@whu.edu.cn+86 27 88041911

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026