A Study to Detect Hyperkalemia Using Smartphone-enabled EKG

Overview

About this study

The purpose of this study is to validate the real-world performance of our previously developed AI-ECG algorithm for identification of hyperkalemia with a six-lead mobile-enhanced device  

Ambulatory adult patients at increased risk for hyperkalemia due to age ≥ 50 years, and one or more criteria including eGFR (from serum creatinine) < 45 ml/minute and/or a history of serum potassium > 5.2 mEq/l, who present to the emergency department will be approached to consent for our rapid screening process.

 

 

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:

  • Age greater than/equal to 50 years and able to provide consent.
  • Patients with eGFR (from serum creatinine) < 45 ml/minute and/or a history of serum potassium > 5.2 mEq/l.

Exclusion Criteria:

  • Patients underage < 50.
  • Do not meet inclusion criteria.
  • Unstable patients requiring emergent resuscitation.
  • Patients unable to provide consent.

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 Dillon, M.D.

Closed-enrolling by invitation

What is this? (?)
"Close"
Not open to everyone who meets the eligibility criteria, but only those invited to participate by the study team.

Contact information:

Jennifer Dugan

(507) 538-1125

Dugan.Jennifer@mayo.edu

More information

Publications

Publications are currently not available
.
CLS-20533029

Mayo Clinic Footer