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Multi-center study of natural course of hereditary retinal diseases

Multi-center study of natural course of hereditary retinal diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000034611
Enrollment
Unknown
Registered
2020-07-12
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-07-13

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

Conditions

inherited retinal dystrophy

Interventions

Case series:Nil

Sponsors

Shanghai Childrens Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. IRDS patients with confirmed gene mutation / translocation / deletion; 2. Aged 4-18years; 3. Sign informed consent; 4. Complete 4 basic eye examinations: corrected visual acuity; fundus photography; Oct; ERG

Exclusion criteria

Exclusion criteria: 1. Failure to follow study or follow-up procedures; 2. It has participated in other intervention treatment studies, such as new drugs, stem cell therapy and transgenic treatment; 3. Patients with severe systemic diseases, mental retardation, mental illness, etc., who can not accept eye examination; 4. There are traumatic retinopathy, retinal inflammatory disease, paraneoplastic retinopathy, drug toxicity and rare diseases, such as diffuse unilateral subacute optic nerve retinitis; 5. At the first visit, both eyes showed no light perception; 6. Both eyes have a history of intraocular surgery; 7. The researchers believe that they need to be excluded.

Design outcomes

Primary

MeasureTime frame
The proportion of deterioration in natural course of follow-up in patients with IRDS;

Countries

China

Contacts

Public ContactTong Qiao

Department of Ophthalmology, Shanghai Children‘s Hospital

qiaojoel@163.com+86 18901600271

Outcome results

None listed

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