Predicting Complications in Women With Toxaemia
NCT00175526 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 650
Last updated 2016-06-01
Summary
At present, the management of pre-eclampsia is guided by expert opinions that are not well-based on firm evidence. What is required is a clinical tool that can accurately determine a women's risk for adverse outcomes, and thereby reduce the risk for women while safely prolonging pregnancies remote from term (to improve fetal outcomes). This research project, 'a severity score for pre-eclampsia,' will develop such a clinical tool that is specific to the condition. This severity score will be used clinically (to guide management) and in research (in both clinical trials and basic science research), and will provide an evidence base on which to build future practice, improving outcomes for pregnant women and their babies. In addition, this project is part of a three part strategy to better understand the mechanisms of disease in pre-eclampsia and to investigate a potential disease-modifying therapy, namely, recombinant human activated protein C.
Conditions
- Toxemia
Interventions
- BEHAVIORAL
-
preeclampsia
This research project, 'a severity score for pre-eclampsia,' will develop such a clinical tool that is specific to the condition. To develop and validate the tool w
Sponsors & Collaborators
-
University of British Columbia
lead OTHER
Principal Investigators
-
Peter von Dadelszen, MD · University of British Columbia
Eligibility
- Min Age
- 16 Years
- Max Age
- 45 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2005-09-30
- Primary Completion
- 2010-12-31
- Completion
- 2010-12-31
Countries
- Canada
- New Zealand
- United Kingdom
Study Locations
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