Using a Novel Transdermal Infrared Spectroscopic Device Correlation of Plasma High Sensitivity Cardiac Troponin T and Cardiac Troponin

Overview

About this study

The goal of this study is to assess the correlation of the cardiac troponin values obtained using this sensor compared to our currently used lab measurement, which is the high-sensitivity cardiac troponin T (hs-cTnT) by Roche Diagnostics. 

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:

  • Adult males or females that present to the emergency department and have serial plasma hs-cTnT performed as a routine part of their care.
  • Age 18 years or older.
  • Able to provide written informed consent.

Exclusion Criteria: 

  • Acutely ill patients in need or rapid intervention/care.
  • Those unable to provide written informed consent because of lack of capacity or unconsciousness.

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

Leslie Donato, Ph.D.

Open for enrollment

Contact information:

Ronstan Lobo M.B., B.Ch., B.A.O.

(507) 284-8586

Lobo.Ronstan@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20545767

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