Blood Volume Measurement using HES injection, and Noninvasive Cardiac Output Measurement to Assess Hemodynamic Responses During Elective Cesarean Section.

Withdrawn

• Conditions: hemodynamiek; cesarean section; surgical birth; 10026906; 10029903

• Registration Number: NL-OMON46850
• Lead Sponsor: Medisch Universitair Ziekenhuis Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 158

Inclusion Criteria

-pregnant women scheduled for elective cesarean section
-over 18 years of age
-singleton pregnancy
-agree to participate in the study
-mastery of the Dutch language

Exclusion Criteria

-under 18 years of age
-multiple pregnancy
-cardiac disease: pump failure, congenital defects with ongoing hemodynamic effects (valve dysfunction)
-refusal to participate in the study

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Primary endpoint is severe hypotension, defined as either a decline in blood<br /><br>pressure of 20% ore more from the baseline, or a systolic blooed pressure below<br /><br>100 mmHg. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary enpoints will be the relative changes in cardiac output during volume<br /><br>resuscitation.</p><br>