To study retina of preterm infants with retinal imaging system
Not Applicable
- Conditions
- Health Condition 1: H351- Retinopathy of prematurity
- Registration Number
- CTRI/2019/07/020188
- Lead Sponsor
- Goverment medical college and hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All Inborn babies with birth weight less than or equal to 1750 grams and period of gestation less than or equal to 32 weeks or if the baby is referred to ROP screening by neonatologist will be screened and babies with ROP will be included in this study
Exclusion Criteria
Corneal opacity or hazy media precluding FFA Patients with :
a) Renal failure b) Allergic reaction to dye sodium fluorescein c) Neonate on respiratory support d) Major congenital abnormality e) TORCH infections suspicion on eye examination
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method FFA predictors of progression of Retinopathy of prematurityTimepoint: At time of presentation
- Secondary Outcome Measures
Name Time Method vascular changes of retina on FFA after treatmentTimepoint: 6 month after treatment