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NCT02383667 Clinical Trial

Clinical Comparison of Electrocardiograms Collected Using an Ambulatory Holter

Electrocardiography Clinical Trial

— Orbital  

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02383667
Other study ID # Orbital
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2013
Est. completion date May 2015

Study information
Verified date September 2019
Source University of Toledo Health Science Campus
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date May 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Related Conditions & MeSH terms

Intervention

Device:
• Electrocardiogram holter

Locations
Country Name City State
United States University of Toledo, Health Science Campus Toledo Ohio

Sponsors (1)
Lead Sponsor Collaborator
University of Toledo Health Science Campus

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Arrythmia 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		 15 minutes
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