Monitoring Arrhythmia Patients (IMPACT)

NCT ID: NCT00919568

Last Updated: 2010-02-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

28 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-06-30

Study Completion Date

2009-11-30

Brief Summary

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

Detailed Description

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

Conditions

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Arrhythmias

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Corventis, Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Corventis

Principal Investigators

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Imad Libbus, PhD

Role: STUDY_DIRECTOR

Corventis, Inc.

Locations

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Dr. Bedi

Steubenville, Ohio, United States

Site Status

Countries

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United States

Other Identifiers

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COR-2009-005

Identifier Type: -

Identifier Source: org_study_id

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