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Clinical Trials/NCT02383667
NCT02383667
Completed
Not Applicable

Clinical Comparison of Electrocardiograms Collected Using an Ambulatory Holter

University of Toledo Health Science Campus1 site in 1 country20 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Electrocardiography
Sponsor
University of Toledo Health Science Campus
Enrollment
20
Locations
1
Primary Endpoint
Arrythmia
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The objective of the study is to compare electrocardiograms using ambulatory holter monitor with dry electrodes in a harness versus using an ambulatory holter with standard sticky electrodes (Red Dot) on monitored patients within the hospital. Patients will be simultaneously be hooked up to two ambulatory Holter monitors for the period of time to be not less than one hour. One holter will use standard electrodes in a standard electrode distribution. The second holter will use dry electrodes in a derived.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
May 2015
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University of Toledo Health Science Campus
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Any patient within the hospital either for procedure or for admission

Exclusion Criteria

  • Patients who cannot wear a Holter monitor
  • Patients undergoing an MRI or have other contraindications for wearing an ambulatory Holter monitor.

Outcomes

Primary Outcomes

Arrythmia

Time Frame: 15 minutes

quality of data obtained between harness and holter. Subjective evaluation: -Quality of the data will be rated on a 0 - 10 scale with 0 being unreadable and 10 being excellent

Study Sites (1)

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