Common Sensing and Right Ventricular Automatic Capture (COGNATE)

Completed

Conditions studied: Bradycardia, Chronotropic Incompetence

In brief

This study will collect data on features for future pacemakers via an external non-implantable system.

Key facts

Study ID

NCT01030705

Run by

Boston Scientific Corporation

People needed

80

Starts

2009-11-01

Expected to finish

2010-06-01

Last updated by the study team

2011-09-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients who are scheduled to receive either Pacemaker (dual chamber) or CRT-P devices based on physician discretion
• Patients who are willing and capable of participating in all testing associated with this Clinical Investigation
• Patients who are age 18 or above, or of legal age to give informed consent specific to state and national law

You may not qualify if…

• Patient enrolled in any concurrent study, without Boston Scientific CRM written approval, that may confound the results of this study
• Patients with a prosthetic mechanical tricuspid heart valve
• Women who are pregnant

Where it is running

• St. Luke's Hospital — Cedar Rapids, Iowa, United States
• Nebraska Heart Institute — Lincoln, Nebraska, United States
• University of Pittsburgh Medical Center, Cardiac Electrophysiology — Pittsburgh, Pennsylvania, United States
• Intermountain Medical Center — Murray, Utah, United States
• Virginia Commonwealth University Health System, Medical College of Virginia, MCV Physicians and Hospitals — Richmond, Virginia, United States

Full record on ClinicalTrials.gov

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