NCT01178541

Brief Summary

Study designed to measure simultaneously the width of both lateral ventricles of the fetal brain. Thus, will enable to evaluate the normal asymmetry that may exist between the right and the left ventricles during the pregnancy.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2010

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 8, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 10, 2010

Completed
2 months until next milestone

Study Start

First participant enrolled

October 1, 2010

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2012

Completed
Last Updated

February 20, 2013

Status Verified

March 1, 2012

Enrollment Period

2.2 years

First QC Date

August 8, 2010

Last Update Submit

February 18, 2013

Conditions

Healthy

Keywords

ventriclesfetalbrainasymmetry

Outcome Measures

Primary Outcomes (1)

  • width of lateral ventricles along the pregnancy

    constructing a graph of the width of the lateral ventricles according to the gestational weeks

    one year

Eligibility Criteria

Age18 Years - 50 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

low risk pregnant women

You may qualify if:

  • low risk pregnant women

You may not qualify if:

  • high risk pregnant women

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Rotshild Women Health Center

Petah Tikva, Israel

Location

Study Officials

  • David Vardimon, MD

    Clalit Health Services

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 8, 2010

First Posted

August 10, 2010

Study Start

October 1, 2010

Primary Completion

December 1, 2012

Study Completion

December 1, 2012

Last Updated

February 20, 2013

Record last verified: 2012-03

Locations

IL(1)