N/A
N=30
LiDCO Monitor Study
Cardiac Surgery
Bottom Line
View on ClinicalTrials.gov: NCT01567371 ↗Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Apr 2016
Primary outcome: Primary: Difference in Pulse Pressure Variability From Baseline to Post-ANH — 7.46 % variability
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- LiDCO rapid monitor (Device)
- Age
- Pediatric, Adult, Older Adult
- Sex
- All
- Sponsor
- Nationwide Children's Hospital
- Primary completion
- Dec 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Difference in Pulse Pressure Variability From Baseline to Post-ANH |
7.46 | — |
| SECONDARY Difference in Stroke Volume Variability From Baseline to Post ANH. |
4.46 | — |
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.
Eligibility Criteria
Inclusion Criteria
- Patients scheduled for intraoperative phlebotomy following anesthetic induction to obtain autologous blood for use following cardiopulmonary bypass and cardiac surgery.
Data sourced from ClinicalTrials.gov (NCT01567371). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.