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Estimating Blood [Lactate] Non-Invasively

Overview

About this study

The purpose of this study is to validate the LabClasp’s ability to estimate blood [lactate].

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 - Aim 1:

  • Subjects must be able to provide written consent. 
  • Adults 18 years of age and older.
  • Nonsmokers.
  • No recent hospitalization (< 60 days).
  • Ability to perform high-intensity exercise.

Inclusion Criteria - Aim 2:

  • Subjects must be able to provide written consent to be included in the research study.
  • Adults 18 years of age and older.
  • Nonsmokers.
  • Current ICU patient.
  • Have regular blood samples taken for [lactate] measurements.
  • Have one or more risk factors for sepsis.

Exclusion Criteria - Aims 1 and 2:

  • History of, or active malignancy.
  • History of HIV with antiretroviral treatment.
  • Smokers.
  • Pregnancy.

 

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

Virend Somers, M.D., Ph.D.

Contact us for the latest status

Contact information:

Miranda Jones

(507) 422-1583

Jones.Miranda@mayo.edu

More information

Publications

Publications are currently not available

More about research at Mayo Clinic

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CLS-20521240

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