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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03277417
Other study ID # HYMC-0037-17
Secondary ID
Status Not yet recruiting
Phase N/A
First received August 30, 2017
Last updated September 6, 2017
Start date September 2017
Est. completion date September 2019

Study information

Verified date September 2017
Source Hillel Yaffe Medical Center
Contact Rinat Gabbay-Benziv, MD
Phone 972-4-6304512
Email rinatg@hy.health.gov.il
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To evaluate and compare fetal cardiac performance by fetal echocardiography and delivery outcome between fetuses with isolated oligohydramnios, normal amniotic fluid and polyhydramnios.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 90
Est. completion date September 2019
Est. primary completion date September 2019
Accepts healthy volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Gestational age 24-42 weeks

- Singleton pregnancies

Exclusion Criteria:

- Fetal anatomical or chromosomal abnormality

- Known fetal cardiac defect

- Suspected fetal infection

- Suspected IUGR

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Echocardiography
Imaging of fetal heart and amniotic fluid

Locations

Country Name City State
Israel Hillel Yaffe Medical Center H_adera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fetal cardiac ventricles The width of the fetal cardiac ventricles will be measured and compared between all three groups One month
Secondary Gestational age Gestational age at delivery will be compared between the three groups One month
Secondary Mode of delivery Mode of delivery will be compared between the three groups One month
Secondary Birth weight Birth weight will be compared between the three groups One month
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