Clinical Trial: P3: Pacemaker Patient Profiling Study

Study Status: Terminated
Recruit Status: Terminated
Study Type: Observational

Official Title: Pacemaker Patient Profiling (P3) Study

Brief Summary: The P3 Study is a United States post market study to gather data on clinical status, primary indications, device therapy choices, clinical management and outcomes for patients with implantable pacemakers.

Detailed Summary:
Sponsor: Medtronic Cardiac Rhythm and Heart Failure

Current Primary Outcome:

• Number of Participants With Dual Chamber Devices [ Time Frame: at original implant ]
  Pacemaker device choice characterized by the number of patients with dual chamber devices
• Days Hospitalized [ Time Frame: implant to one year ]
  Healthcare utilization clinical outcome characterized by number of days hospitalized in the first year
• Multiple In-clinic Visits [ Time Frame: implant to one year ]
  Follow-up practice pattern assessed by the number of patients with a dual chamber device that had two or more routine pacemaker in-clinic visits with a device interrogation

Original Primary Outcome:

Current Secondary Outcome:

Original Secondary Outcome:

Information By: Medtronic Cardiac Rhythm and Heart Failure

Dates:
Date Received: February 16, 2006
Date Started: March 2004
Date Completion:
Last Updated: April 6, 2011
Last Verified: April 2011