N/A Completed N=30 Diagnostic

LiDCO Monitor Study

Cardiac surgery

Source: ClinicalTrials.gov NCT01567371 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Apr 2016

Primary outcomePrimary: Difference in Pulse Pressure Variability From Baseline to Post-ANH — 7.46 % variability

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.

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	—

Eligibility Criteria

Inclusion Criteria

Patients scheduled for intraoperative phlebotomy following anesthetic induction to obtain autologous blood for use following cardiopulmonary bypass and cardiac surgery.

View full record on ClinicalTrials.gov →

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. Informational only — not medical advice.