Trials / Completed
CompletedNCT04537065
Long Term Outcome of Intravitreal Ranibizumab for ROP
Refractive and Biometric Outcome Following Intravitreal Injection of Ranibizumab in Retinopathy of Prematurity: Long -Term Study
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 140 (actual)
- Sponsor
- Ameera Gamal Abdelhameed · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
premature infants who had a history of intravitreal injection of (Ranibizumab) not less than one year were examined for refractive state and biometry
Detailed description
Medical records were collected in each group for birth history data, including gestational age (GA), birth weight (BW), and postmenstrual age (PMA) at time of intravitreal injection. The zone and stage of ROP were also recorded. All patients were evaluated for refractive errors and cycloplegic refraction was performed using a handheld auto keratorefractometer (Righton Retinomax K-plus2), and confirmed by retinoscopy examination. Refractive errors were calculated as spherical equivalent and astigmatism in cylinder. The average corneal radius of curvature was measured by handheld auto kerato-refractometer (Righton Retinomax K-plus2). The biometric optic components, including anterior chamber depth, lens thickness, and axial length, were measured using A-scan ultrasound (model Echoscan US-4000 / 500; Nidek)
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | cycloplegic refraction | Cycloplegic refraction and the average corneal radius of curvature were performed using a handheld auto kerato-refractometer (Righton Retinomax K-plus2). Refraction was confirmed by retinoscopy and refractive errors were calculated as spherical equivalent and astigmatism in cylinder. The biometric optic components, including anterior chamber depth, lens thickness, and axial length, were measured using A-scan ultrasound (model Echoscan US-4000 / 500; Nidek). |
Timeline
- Start date
- 2018-04-01
- Primary completion
- 2018-09-01
- Completion
- 2018-09-01
- First posted
- 2020-09-03
- Last updated
- 2020-09-03
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04537065. Inclusion in this directory is not an endorsement.