LiDCO Monitor Study
Not Applicable
Completed
- Conditions
- Cardiac Surgery
- Interventions
- Device: LiDCO rapid monitor
- Registration Number
- NCT01567371
- Lead Sponsor
- Nationwide Children's Hospital
- Brief Summary
This is a study to validate the utility and accuracy of the non-invasive device (LiDCOrapid monitor) during a period of phlebotomy and graded blood loss in patients who are having cardiac surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
- Patients scheduled for intraoperative phlebotomy following anesthetic induction to obtain autologous blood for use following cardiopulmonary bypass and cardiac surgery.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description LiDCO rapid monitor LiDCO rapid monitor -
- Primary Outcome Measures
Name Time Method Difference in Pulse Pressure Variability From Baseline to Post-ANH 1 Day The difference in pulse pressure variability during a period of phlebotomy and graded blood loss, measured before phlebotomy or acute normovolemic hemodilution (ANH) and immediately after.
- Secondary Outcome Measures
Name Time Method Difference in Stroke Volume Variability From Baseline to Post ANH. 1 Day The difference in stroke volume variability during a period of phlebotomy and graded blood loss, measured before phlebotomy or acute normovolemic hemodilution (ANH) and immediately after.
Trial Locations
- Locations (1)
Nationwide Children's Hospital
🇺🇸Columbus, Ohio, United States