Monitoring Arrhythmia Patients in in Hospital Monitoring (ADAM)

This study has been completed.
Sponsor:
Information provided by:
Corventis, Inc.
ClinicalTrials.gov Identifier:
NCT00919646
First received: June 10, 2009
Last updated: February 2, 2010
Last verified: February 2010
  Purpose

This is a prospective, single center, non-randomized study to evaluate the arrhythmia monitoring performance of the AVIVO™ System in a hospital setting.


Condition
Arrhythmias

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

Resource links provided by NLM:


Further study details as provided by Corventis, Inc.:

Estimated Enrollment: 30
Study Start Date: April 2009
Study Completion Date: October 2009
Primary Completion Date: October 2009 (Final data collection date for primary outcome measure)
Detailed Description:

The AVIVO™ System will continuously monitor the patient's cardiac activity which will be compared to the performance of standard telemetry 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

Telemetry ward

Criteria

Inclusion Criteria:

  • Is female or male, 18 years of age or older
  • Undergoing in-hospital electrocardiographic monitoring for primarily cardiac reasons

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: NCT00919646

Sponsors and Collaborators
Corventis, Inc.
Investigators
Study Director: Imad Libbus, PhD Corventis, Inc.
  More Information

No publications provided

Responsible Party: Madhuri Bhat, VP Regulatory and Clinical affairs, Corventis
ClinicalTrials.gov Identifier: NCT00919646     History of Changes
Other Study ID Numbers: COR-2009-001
Study First Received: June 10, 2009
Last Updated: February 2, 2010
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Arrhythmias, Cardiac
Heart Diseases
Cardiovascular Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on August 28, 2014