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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00199810
Other study ID # Elangepreeklampsi2005-
Secondary ID S-05173
Status Completed
Phase Phase 4
First received September 15, 2005
Last updated October 14, 2016
Start date July 2005
Est. completion date August 2008

Study information

Verified date October 2016
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Medicines Agency
Study type Observational

Clinical Trial Summary

This trial is examining hemodynamic measurements in women with serious preeclampsia.


Recruitment information / eligibility

Status Completed
Enrollment 68
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Women with serious preeclampsia

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Norway Oslo University Hospital Oslo

Sponsors (1)

Lead Sponsor Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Hemodynamic variations in preeclamptic women days No
Secondary Urine output days No
Secondary thrombocyte count days No
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