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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00943189
Other study ID # SHEBA-08-4934-LG-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received July 21, 2009
Last updated November 19, 2009
Start date June 2008

Study information

Verified date November 2009
Source Sheba Medical Center
Contact Liat Gindes, MD
Email gindesl@smile.net.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

Purpose: Fetal anomalies scan at the time of Nuchal Translucency (NT) study.


Description:

Prospective study of patients at 12-14 weeks gestation that are coming for NT examination is conducted. Meticulous ultrasound examination will be done to the fetuses using trans vaginal and transabdominal techniques. The patients will receive only the NT information. Only in cases of detection of severe fetal anomalies the patient will get the information of the examination and counseling according to the findings. All patients will be asked to provide information of the 15 weeks early comprehensive ultrasound examination. The NT examination will be compared to the 15 weeks ultrasound. All patients will be asked to give information after delivery of the baby's health condition.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- pregnant women at 12-14 weeks

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba Medical Center Ramat Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

See also
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