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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01068002
Other study ID # 071-09-EMC
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2009
Est. completion date September 2012

Study information

Verified date February 2020
Source HaEmek Medical Center, Israel
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cardiovascular & echocardiographic assessment in pregnant women with hypertension during their pregnancy in comparison to Pregnant normotensive women.


Description:

Cardiovascular & echocardiographic assessment in pregnant women with hypertension during their pregnancy in comparison to Pregnant normotensive women. Also,comparing echocardiographic parameters in hypertensive pregnant women being treated with either alfa methyl dopa or labetolol.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date September 2012
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- hypertension during pregnancy: Chronic or pregnancy induced

Exclusion Criteria:

- Inability to sign informed consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Ha'Emek Medical Center Afula

Sponsors (1)

Lead Sponsor Collaborator
HaEmek Medical Center, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hypertension impact on cardiovascular echocardiographic parameters and obstetric parameters in pregnant women with or without treatment 1 year
Secondary Primary outcome, Impact of alfa methyl dopa and labetolol on cardiovascular parameters in pregnant women 1 Year
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