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OpenTrials
Completed

NCT Number: NCT00201500

Left Ventricular and Endothelial Function in Preeclampsia

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.

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Observational

Primary location

NTNU

Trondheim, N-7491, Norway

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Left Ventricular Function

    Time frame: 3 months

  2. Endothelial Function

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Norwegian University of Science and Technology

Other

Collaborators

  • Helse Nord-Trøndelag HF

Registry information

Official study title

Left Ventricular and Endothelial Function in Preeclampsia, a Case Control Study

Important dates

Study start
2004
Primary completion
2005
Study completion
2006
First posted
Sep 20, 2005
Registry last updated
Aug 4, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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