Data Collection from Continuous Non-Invasive Blood Pressure

Overview

About this study

The purpose of this study is to collect data to develop the Masimo INVSENSOR00056 device. The noninvasive blood pressure measurements will be compared to reference arterial blood pressure measurements.

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:

  • 18 years of age or older. 
  • Patients scheduled for an elective surgical procedure requiring the use of an arterial pressure monitoring catheter. 

Exclusion Criteria:

  • Pregnant or lactating women.
  • Subjects with excess body hair on the wrist area.
  • Subjects with abnormal radial or ulnar pathology.
  • Subjects whose skin is not intact in or at the vicinity of the sensor placement site.
  •  Subjects who have any mdical condition which in the judgement of the investigator and/or study staff, renders them ineligible ofr participation in this study or subjects deemed ineligible by the discretion of the investigator/study staff. 

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 3/16/23. Questions regarding updates should be directed to the study team contact.

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

Jacksonville, Fla.

Mayo Clinic principal investigator

Klaus Torp, M.D.

Contact us for the latest status

Contact information:

Ilana Logvinov D.N.P.

Logvinov.Ilana@mayo.edu

More information

Publications

Publications are currently not available