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Outcome of Babies With Asymetry of Lateral Brain Ventricles

NCT ID: NCT01724281

Last Updated: 2012-11-09

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

10 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-12-31

Study Completion Date

2014-12-31

Brief Summary

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The investigators will follow up on babies that had prenatal diagnosis at 2nd or 3rd trimester of normal width and asymetry of lateral brain ventricles

Detailed Description

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Women who will attend 2nd or 3rd ultrasound prenatal scans will be included. Women where the fetus would be diagnosed with lateral ventricles that are normal width (\<10 m"m) but discrepacy of \>3 m"m will be followed up after delivery by head ultrasound and neurologic exam

Conditions

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Lateral Ventricles of Fetuses at Mid Trimester

Keywords

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lateral ventricles Asymetry

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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pregnant women between 19-30 weeks gestational age

No intervention, only follow up

No intervention, only follow up

Intervention Type OTHER

Interventions

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No intervention, only follow up

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthy pregnant women between 19-30 weeks gestational age and asymetry of lateral ventricles

Exclusion Criteria

* Lateral ventricles \>10 m"m
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Hillel Yaffe Medical Center

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hillel Yaffe Medical Center

Hadera, , Israel

Site Status

Countries

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Israel

Central Contacts

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Alon Shrim, MD

Role: CONTACT

Phone: +972506246988

Email: [email protected]

Facility Contacts

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Alon Shrim, MD

Role: primary

Other Identifiers

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0059-12

Identifier Type: -

Identifier Source: org_study_id