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Correlation of Volumetric Brain Analysis With Development at 18 Months

This study has been withdrawn prior to enrollment.
(No data. Study never completed.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00194831
First Posted: September 19, 2005
Last Update Posted: June 15, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Weill Medical College of Cornell University
  Purpose
The study will correlate the volumes of the brain obtained from magnetic resonance imaging (MRI) scans done at term gestation for infants born prematurely who weighed less than 1000 grams at birth with their corresponding development at 18 months corrected age.

Condition
Child Development

Study Type: Observational
Study Design: Observational Model: Cohort
Official Title: Volumetric Brain Analysis in the Premature Brain: Correlation With Future Development

Further study details as provided by Weill Medical College of Cornell University:

Enrollment: 0
Study Start Date: June 2005
Study Completion Date: June 2015
Primary Completion Date: June 2015 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Months to 2 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Premature infants < 1000 gram birthweight who are followed post discharge as part of standard clinical care
Criteria

Inclusion Criteria:

  • All premature infants born < 1000 grams who had MRI scans of the brain at term gestation

Exclusion Criteria:

  • Any known genetic or chromosomal abnormalities
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00194831


Locations
United States, New York
New York Presbyterian Hospital Weill Cornell
New York, New York, United States, 10021
Sponsors and Collaborators
Weill Medical College of Cornell University
Investigators
Study Chair: Jeffrey M Perlman, MB New York Presbyterian Hospital Weill Cornell
  More Information

Responsible Party: Jeffrey Perlman, Weill Cornell
ClinicalTrials.gov Identifier: NCT00194831     History of Changes
Other Study ID Numbers: 000501007693
First Submitted: September 12, 2005
First Posted: September 19, 2005
Last Update Posted: June 15, 2015
Last Verified: June 2015


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