Measurement of Echogenic Area in the Border of the Fetal Ventricles

This study is currently recruiting participants.

Verified March 2012 by Meir Medical Center

Sponsor:

Information provided by (Responsible Party):

Meir Medical Center

ClinicalTrials.gov Identifier:

NCT01178606

First received: August 8, 2010

Last updated: March 16, 2012

Last verified: March 2012

History of Changes

Tracking Information
First Received Date ^ICMJE	August 8, 2010
Last Updated Date	March 16, 2012
Start Date ^ICMJE	September 2010
Primary Completion Date	February 2011 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE	Not Provided
Original Primary Outcome Measures ^ICMJE	Not Provided
Change History	Complete list of historical versions of study NCT01178606 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE	Not Provided
Original Secondary Outcome Measures ^ICMJE	Not Provided
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Measurement of Echogenic Area in the Border of the Fetal Ventricles
Official Title ^ICMJE	Not Provided
Brief Summary	Sonographic coronal section in the lateral fetal ventricles shows echogenic area in the ventricles borders creating an "halo" around the ventricles. Histologically this area correlates to the Stratified transitional field. In this study we would like to measure this area for the purpose of creating a nomogram.
Detailed Description	Not Provided
Study Type ^ICMJE	Observational
Study Design ^ICMJE	Observational Model: Case-Only
Target Follow-Up Duration	Not Provided
Biospecimen	Not Provided
Sampling Method	Probability Sample
Study Population	pregnant women 22-37GA, singleton normal pregnancy
Condition ^ICMJE	Healthy
Intervention ^ICMJE	Not Provided
Study Group/Cohort (s)	Not Provided
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Recruiting
Estimated Enrollment ^ICMJE	150
Estimated Completion Date	November 2012
Primary Completion Date	February 2011 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	Inclusion Criteria: pregnant women 22-37 GA well dated pregnancy singleton pregnancy Exclusion Criteria: no first trimester dating multifetal pregnancy known CNS abnormalities in the fetus small for gestational age
Gender	Both
Ages	22 Weeks to 37 Weeks
Accepts Healthy Volunteers	Yes
Contacts ^ICMJE	Not Provided
Location Countries ^ICMJE	Israel

Administrative Information
NCT Number ^ICMJE	NCT01178606
Other Study ID Numbers ^ICMJE	MMC10094-2010CTIL
Has Data Monitoring Committee	No
Responsible Party	Meir Medical Center
Study Sponsor ^ICMJE	Meir Medical Center
Collaborators ^ICMJE	Not Provided
Investigators ^ICMJE	Not Provided
Information Provided By	Meir Medical Center
Verification Date	March 2012
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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