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NCT03334513
Refractive Error and Biometry in Retinopathy of Prematurity
trial testing Bevacizumab in Retinopathy of Prematurity in 35 participants. Completed in 1 April 2014.
1 April 2014
Quick facts
| Lead sponsor | San Ni Chen |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 35 |
| Start date | 1 April 2011 |
| Primary completion | 1 April 2014 |
| Estimated completion | 1 April 2014 |
Drugs / interventions tested
- Bevacizumab (Bevacizumab-Bvzr) — full drug profile →
- Ranibizumab — full drug profile →
Conditions studied
- Retinopathy of Prematurity — all drugs for Retinopathy of Prematurity →
Sponsor
San Ni Chen
Who can join
Adults 3 to 3, any sex, with Retinopathy of Prematurity. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The investigators compared long-term refractive and biometric outcomes in children with retinopathy of prematurity who received two different anti-vascular endothelial growth factor agents.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Refractive and Biometric Outcomes in Patients with Retinopathy of Prematurity Treated with Intravitreal Injection of Ranibizumab as Compared with Bevacizumab: A Clinical Study of Correction at Three Years of Age.
Chen YC, Chen SN, Yang BC, Lee KH, et al · · 2018 · cited 16× · PMID 29713524 · DOI 10.1155/2018/4565216
Verify or expand the search:
- PubMed search for NCT03334513
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other recruiting trials for Retinopathy of Prematurity
Currently open trials in the same condition.
- NCT05558059 — Imaging Retinal Vasculature in Infant Eyes · recruiting
- NCT06672913 — Impact of Standardized Skin-to-Skin Care on Clinical Outcomes in Infants Born ≤ 32 Weeks: A Multicenter Study · NA · recruiting
- NCT06109285 — Validation of i-ROP DL to Detect More Than Mild ROP · NA · active not recruiting
- NCT06315556 — An Observational Study to Collect Data on How Aflibercept (Eylea) Given Using a Paediatric Dosing Device is Used in Pret · recruiting
- NCT06265363 — Evaluation of the Frequency, Risk Factors, and Outcomes of ROP in Infants With a BW >1500 Grs or GA ≥33 Wks in Turkey. · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03334513 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by San Ni Chen
- Last refreshed: 7 November 2017
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03334513.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing