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Clinical Comparison of Electrocardiograms Collected Using an Ambulatory Holter

Completed
Conditions
Electrocardiography
Registration Number
NCT02383667
Lead Sponsor
University of Toledo Health Science Campus
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Arrythmia15 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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Toledo, Health Science Campus

🇺🇸

Toledo, Ohio, United States

University of Toledo, Health Science Campus
🇺🇸Toledo, Ohio, United States
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