Study Results
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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COMPLETED
35 participants
OBSERVATIONAL
2002-01-31
2003-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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DEFINED_POPULATION
OTHER
Eligibility Criteria
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Inclusion Criteria
* Birth weight \< 1500 gram
* Written informed consent of parents
Exclusion Criteria
* Chromosomal abnormalities
32 Weeks
ALL
No
Sponsors
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Amsterdam UMC, location VUmc
OTHER
Principal Investigators
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R M van Elburg, MD, PhD
Role: STUDY_DIRECTOR
Amsterdam UMC, location VUmc
Other Identifiers
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HK0607
Identifier Type: -
Identifier Source: org_study_id