Monitoring Arrhythmia Patients (IMPACT)

This study has been completed.
Sponsor:
Information provided by:
Corventis, Inc.
ClinicalTrials.gov Identifier:
NCT00919568
First received: June 10, 2009
Last updated: February 2, 2010
Last verified: February 2010
  Purpose

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


Condition
Arrhythmias

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Arrhythmia Detection With Adherent Patient Monitoring

Further study details as provided by Corventis, Inc.:

Enrollment: 28
Study Start Date: June 2009
Study Completion Date: November 2009
Primary Completion Date: November 2009 (Final data collection date for primary outcome measure)
Detailed Description:

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

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Remote cardiac monitoring

Criteria

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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00919568

Locations
United States, Ohio
Dr. Bedi
Steubenville, Ohio, United States, 43952
Sponsors and Collaborators
Corventis, Inc.
Investigators
Study Director: Imad Libbus, PhD Corventis, Inc.
  More Information

No publications provided

Responsible Party: Madhuri Bhat, VP Clinical and Regulatory affairs, Corventis
ClinicalTrials.gov Identifier: NCT00919568     History of Changes
Other Study ID Numbers: COR-2009-005
Study First Received: June 10, 2009
Last Updated: February 2, 2010
Health Authority: United States: Institutional Review Board

ClinicalTrials.gov processed this record on September 22, 2014