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.
Study Type
OBSERVATIONAL
Enrollment
2,013
Number of Participants With Dual Chamber Devices
Pacemaker device choice characterized by the number of patients with dual chamber devices
Time frame: at original implant
Days Hospitalized
Healthcare utilization clinical outcome characterized by number of days hospitalized in the first year
Time frame: implant to one year
Multiple In-clinic Visits
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
Time frame: implant to one year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Birmingham, Alabama, United States
Unnamed facility
Prescott, Arizona, United States
Unnamed facility
Little Rock, Arkansas, United States
Unnamed facility
Aliso Viejo, California, United States
Unnamed facility
Anaheim, California, United States
Unnamed facility
Arcadia, California, United States
Unnamed facility
Escondido, California, United States
Unnamed facility
Fountain Valley, California, United States
Unnamed facility
La Mesa, California, United States
Unnamed facility
Laguna Hills, California, United States
...and 73 more locations