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NCT00919568 Clinical Trial

Monitoring Arrhythmia Patients (IMPACT)

Arrhythmias Clinical Trial

Official title:
Arrhythmia Detection With Adherent Patient Monitoring

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00919568
Other study ID # COR-2009-005
Secondary ID
Status Completed
Phase N/A
First received June 10, 2009
Last updated February 2, 2010
Start date June 2009
Est. completion date November 2009

Study information
Verified date February 2010
Source Corventis, Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

Prospective, multicenter, non-randomized study to determine the performance of NUVANT Mobile Cardiac Telemetry system in arrhythmia detection.

Description:

Arrhythmia patients will be externally monitored. The collected information will be used to evaluate the NUVANT MCT system.

Recruitment information / eligibility
Status Completed
Enrollment 28
Est. completion date November 2009
Est. primary completion date November 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age or older

- Patients undergoing remote ambulatory electrocardiographic monitoring

Exclusion Criteria:

- Is participating in another clinical study that may confound the results of this study

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Dr. Bedi Steubenville Ohio

Sponsors (1)
Lead Sponsor Collaborator
Corventis, Inc.

Country where clinical trial is conducted

United States, 

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