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Clinical Trials/NCT05118022
NCT05118022
Completed
Not Applicable

Artificial Intelligence Identified Dyskalemia Using Electrocardiogram (AIDE) Prompts Immediate Treatment

National Defense Medical Center, Taiwan1 site in 1 country14,989 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hyperkalemia
Sponsor
National Defense Medical Center, Taiwan
Enrollment
14989
Locations
1
Primary Endpoint
Cumulative proportion of hyperkalemia treatment
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This is a randomized controlled trial (RCT) to test a novel artificial intelligence (AI)-enabled electrocardiogram (ECG)-based screening tool for improving the diagnosis and management of potassium abnormalities.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
February 28, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
National Defense Medical Center, Taiwan
Responsible Party
Principal Investigator
Principal Investigator

Chin Lin

Associate Professor

National Defense Medical Center, Taiwan

Eligibility Criteria

Inclusion Criteria

  • Patients in emergency department.
  • Patients recieved at least 1 ECG examination.

Exclusion Criteria

  • Patients recieved dyskalemia-related treatment before ECG examination.
  • The patients recieved ECG at the period of inactive AI-ECG system.

Outcomes

Primary Outcomes

Cumulative proportion of hyperkalemia treatment

Time Frame: Within 3 hours

Calcium supplement, insulin, potassium binding resin, β2-agonist, loop diuretics, sodium bicarbonate, and hemodialysis.

Cumulative proportion of hypokalemia treatment

Time Frame: Within 3 hours

Intravenous potassium chloride, oral potassium gluconate, and oral potassium chloride

Secondary Outcomes

  • Cardiac arrest (sudden death)(Within 3 days)
  • Cumulative proportion of All-cause mortality(Within 365 days)
  • Cumulative proportion of electric shock(Within 6 hours)
  • Cumulative proportion of CPR event(Within 6 hours)
  • Cumulative proportion of Discharge(Within 14 days)
  • Cumulative proportion of Treatment-induced hypokalemia event(Within 24 hours)
  • Cumulative proportion of Treatment-induced hyperkalemia event(Within 24 hours)

Study Sites (1)

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