FindTrial
Sign In

To assess pattern of cerebral visual impairment in children due to genetic v/s acquired causes

Evaluation of pattern of cerebral visual impairment (CVI) in children due to genetic causes v/s acquired causes- A cross sectional study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/01/101171
Enrollment
78
Registered
2026-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: H476- Disorders of visual cortex

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: known case of CVI or newly diagnosed, visiting CVI clinic in KLES Dr. Prabhakar Kore hospital and MRC, Belagavi

Exclusion criteria

Exclusion criteria: 1. caregiver of children not willing to give consent 2. children with no known cause of CVI, not willing for genetic counselling 3. not willing for neuroimaging

Design outcomes

Primary

MeasureTime frame
Pattern of CVI in children with genetic v/s acquired causes of CVITimepoint: at time of evaluation—

Secondary

MeasureTime frame
To analyze spectrum of genetic causes of CVI in south IndiaTimepoint: at time of evaluation—

Countries

India

Contacts

Public ContactDr Smitha K S

Jawaharlal Nehru Medical College, Belagavi

smitha290780@gmail.com8050161268

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026