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. If you need assistance understanding the eligibility criteria, please contact the study team.

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 us for help.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

John Schirger, M.D.

Open for enrollment

Contact information:

Pavol Sajgalik M.D.

(507)255-4426

Sajgalik.Pavol@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20309538

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