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Retinopathy of Prematurity:Summary of a Decade

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01363960
Enrollment
609
Registered
2011-06-02
Start date
1999-03-31
Completion date
2010-12-31
Last updated
2011-06-02

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

Conditions

Retinopathy of Prematurity

Keywords

Incidence, neonatal care, retinopathy of prematurity, risk factors

Brief summary

The aim of the study is to evaluate our 10 year experience of retinopathy of prematurity screening.

Interventions

None listed

Sponsors

Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Neonates either with a BW of less than 1501 gram (g) or born at a GA of 34 weeks (wk) or less * selected infants with an unstable clinical course were included

Design outcomes

Primary

MeasureTime frameDescription
Number of neonates developed retinopathy of prematurityten years
risk factors contributing to ROP developmentten yearsmechanic ventilation. oxygen therapy, respiratory distress syndrome, sepsis, intraventricular, hemorrhage, blood transfusion v.s

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026