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Genetic studies on congenital cataract patients from North-India

Genetic studies on some prevalent vision defects in Aligarh. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/12/078771
Enrollment
25
Registered
2024-12-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: H260- Infantile and juvenile cataract

Interventions

Intervention1: NIL: NIL

Sponsors

University Grants Commission
Lead Sponsor
UGC NonNET
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients diagnosed with congenital cataracts, aged 0-18 years, either unilateral or bilateral, confirmed through clinical examination.

Exclusion criteria

Exclusion criteria: Patients having a history of intrauterine infection (TORCH), toxoplasmosis, others (hepatitis B, syphilis), rubella, cytomegalovirus, Herpes simplex virus; Other ocular clinical manifestations such as glaucoma, microcephaly, micro-opthalamos, uveal coloboma, and retinal disgeneration to rule out any systemic involvement ; Maternal history of steroid uses; Trauma

Design outcomes

Primary

MeasureTime frame
The study is expected to identify novel genetic mutations and provide a better understanding of the genetic and environmental factors contributing to congenital cataracts in North India.Timepoint: One Year

Secondary

MeasureTime frame
Secondary objectives include investigating familial patterns, exploring environmental interactions, & studying genetic variations across different ethnic groups.We also aim to develop genetic counseling guidelines for families at risk.Timepoint: Two Years

Countries

India

Contacts

Public ContactMohammad Afzal

Aligarh Muslim University

aalefatima1425@gmail.com8532851383

Outcome results

None listed

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