High Sensitive Multichannel Non-Invasive Blood Pressure Monitor

Overview

About this study

The objective of this study is to obtain preliminary data to evaluate the accuracy of non-invasive blood pressure measurement in patients supported by continuous-flow left ventricular assist device (LVAD) using non-invasive supra-systolic methods in highly sensitive experimental blood pressure monitor.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Heart failure patients treated by implantation of the continuous flow LVAD as either bridge to transplant or as a destination therapy

Exclusion Criteria:

  • Subjects lacking the capacity to consent
  • Subjects with a Glasgow Coma Scale score below 15

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

John Schirger

Closed for enrollment

Contact information:

John Schirger

(507) 293-1351

Schirger.John@mayo.edu

More information

Publications

Publications are currently not available
.
CLS-20309538

Mayo Clinic Footer