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NCT00682201 Clinical Trial

Hemodynamic Changes During Normal Pregnancy

Pregnancy Clinical Trial

Official title:
Hemodynamic Changes During Normal Pregnancy: A Prospective Cohort Study of 100 Healthy Pregnant Women

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00682201
Other study ID # storkhemo-08-GG
Secondary ID
Status Completed
Phase N/A
First received May 20, 2008
Last updated July 3, 2011
Start date August 2007
Est. completion date June 2009

Study information
Verified date June 2009
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway: Data Protection Authority
Study type Observational

Clinical Trial Summary

Prospective, observational study of the changes in hemodynamic variables such as blood pressure, cardiac output, systemic vascular resistance, and of changes in respiratory variables such as vital capacity, and functional residual volume.A cohort study of 100 healthy pregnant women tested with non-invasive methods during pregnancy and 6 months after delivery.

Description:

Healthy pregnant women with the willingness to consent in physiologic tests at 3 different time points during, and one time point after pregnancy. Spirometric tests will be performed with V-MAX, non-invasive measuring of hemodynamics will be measured by Finometer.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Pregnant women who at first admission are healthy

Exclusion Criteria:

- Co-existing diseases who represents decreased physical or psychological function

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Norway Rikshospitalet University Hospital, Division of Anesthesia and Critical Care Medicine 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 Pregnancy specific changes in hemodynamic variables Normal pregnancy time frame No
Secondary Respiratory functional changes Normal pregnancy time frame No
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