Retinopathy of Prematurity:Summary of a Decade

NCT ID: NCT01363960

Last Updated: 2011-06-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

609 participants

Study Classification

OBSERVATIONAL

Study Start Date

1999-03-31

Study Completion Date

2010-12-31

Brief Summary

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

Detailed Description

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Conditions

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Retinopathy of Prematurity

Study Groups

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neonates with retinopathy of prematurity

all neonates meet the criteria:

1. a BW of less than 1501 gram (g)
2. born at a GA of 34 weeks (wk) or less and
3. selected infants with an unstable clinical course were included

No interventions assigned to this group

Eligibility Criteria

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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
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Saglik Bilimleri Universitesi Gulhane Tip Fakultesi

OTHER

Sponsor Role lead

Responsible Party

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Gulhane Military Medical School

Locations

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Gulhane Military Medical School Training Hospital

Ankara, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Related Links

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http://www.ncbi.nlm.nih.gov/pubmed

retinopathy of prematurity

Other Identifiers

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Retinopathy of prematurity

Identifier Type: -

Identifier Source: org_study_id

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