Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01516697

Non-invasive Cardiac Output Monitoring in Obstetric Patients

Using Thoracic Electrical Bioimpedance to Measure Stroke Volume and Cardiac Output in Patients Under Spinal Anesthesia for Cesarean Section

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Massachusetts General Hospital · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The investigators hypothesize that continuously measuring stroke volume (SV) and cardiac output (CO) will 1) reveal hemodynamic instability in a timely manner and alert the physician promptly, 2) provide information for the physician to make the differential diagnosis as to whether the hemodynamic instability was due to vasodilatation or reduction of venous blood return, and 3) lead to appropriate and prompt treatment to improve patient outcome. -determine the SV and CO and their kinetic change using ICON® to establish a hemodynamic profile of the patient under spinal anesthesia for cesarean section. To determine if using instantaneous measurements of SV and CO to guide patient management improves hemodynamic stability.

Conditions

Interventions

TypeNameDescription
PROCEDUREexperimentalNon-invasive cardiac output monitoring using thoracic electric bioimpedance analysis via ICON® in addition of the standard monitoring during cesarean section.
PROCEDUREControlData obtained from the non-invasive cardiac output monitor,ICON®, are not available for the anesthesia care providers.

Timeline

Start date
2011-10-01
Primary completion
2012-09-01
Completion
2012-09-01
First posted
2012-01-25
Last updated
2017-01-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01516697. Inclusion in this directory is not an endorsement.