- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01360528
Serum Folic Acid Levels in Preterm Infants (FALIPI)
February 15, 2012 updated by: Mehmet Yekta
Zekai Tahir Burak Maternity and Teaching Hospital
Therefore preterm infants must need folic acid replacement than term babies.
Study Overview
Status
Completed
Conditions
Detailed Description
All babies need to different vitamin supplementation.
Especially preterm infants need some vitamin supplements.
Folic acid is very important structure of part of cell growing.ın
theorically; preterm infants have very rapid cell reproduction capacity than term infants.
Therefore preterm infants must need folic acid replacement than term babies.
The investigators want to determine preterm infants folic acid levels due to gestational age whether needs folic acid replacement.
Study Type
Observational
Enrollment (Actual)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ankara, Turkey, 06600
- Zekai Tahir Burak Maternity Teaching Hospital, Neonatology Unit
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
5 months to 7 months (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Extremely low birth weight, Very low birth weight, Low birth weight
Description
Inclusion Criteria:
-All preterm infants
Exclusion Criteria:
-Major congenital anomaly
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Extremely low birth weight
Extremely low birth weight under 1000 gram
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Very low birth weight
Between 1000-1500 gram babies
|
Low birth weight
Between 1500-2500 gram
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
February 1, 2011
Primary Completion (Actual)
May 1, 2011
Study Completion (Actual)
October 1, 2011
Study Registration Dates
First Submitted
May 23, 2011
First Submitted That Met QC Criteria
May 24, 2011
First Posted (Estimate)
May 25, 2011
Study Record Updates
Last Update Posted (Estimate)
February 17, 2012
Last Update Submitted That Met QC Criteria
February 15, 2012
Last Verified
February 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ztb5326315185
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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