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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00201500
Other study ID # PEETLV
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received September 16, 2005
Last updated August 3, 2016
Start date October 2004
Est. completion date March 2006

Study information

Verified date August 2016
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Social Science Data Services
Study type Observational

Clinical Trial Summary

The purpose of this study is (1) to examine whether the left ventricular function is impaired in women with preeclampsia relative to healthy pregnant controls, (2) to examine whether the endothelial function is impaired in women with preeclampsia relative to healthy pregnant controls, and (3) to examine whether there is a post partum impairment in left ventricular and endothelial function.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date March 2006
Est. primary completion date December 2005
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- >18 years of age

- Case: Clinical diagnosis of preeclampsia,

- Control: Systolic BP <140 mmHg and diastolic BP <90 mmHg

Exclusion Criteria:

- Known hypertension or other cardiovascular disease

- Diabetes/gestational diabetes

- Multiple gestation

Study Design

Observational Model: Case Control


Related Conditions & MeSH terms


Locations

Country Name City State
Norway NTNU Trondheim

Sponsors (2)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Central Norway Regional Health Authority

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Tyldum EV, Backe B, Støylen A, Slørdahl SA. Maternal left ventricular and endothelial functions in preeclampsia. Acta Obstet Gynecol Scand. 2012 May;91(5):566-73. doi: 10.1111/j.1600-0412.2011.01282.x. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Left Ventricular Function 3 months No
Primary Endothelial Function 3 months No
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