Personalized CRT - PSR
Status: | Recruiting |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | Any |
Updated: | 10/31/2018 |
Start Date: | January 2012 |
End Date: | January 2024 |
Contact: | PSR Study Team |
Email: | rs.productsurveillanceregistry@medtronic.com |
Phone: | 1-800-633-8766 |
Personalized CRT - Product Surveillance Registry (PSR)
The purpose of this study is to evaluate the cardiac resynchronization therapy (CRT) response
in a real-world patient population and evaluate options to address non-response and patient
management.
in a real-world patient population and evaluate options to address non-response and patient
management.
The Personalized CRT study is a multi-center, single arm, prospective observational study.
The purpose of the study is to better understand and characterize heart failure (HF) patient
management by characterizing the use and clinical benefit of Medtronic market-released
features/tools within the HF Patient Management portfolio.
The purpose of the study is to better understand and characterize heart failure (HF) patient
management by characterizing the use and clinical benefit of Medtronic market-released
features/tools within the HF Patient Management portfolio.
Inclusion Criteria:
- Patient or legally authorized representative provides written authorization and/or
consent per institution and geographical requirements
- Patient has or is intended to receive or be treated with an eligible CRT device
- Patient within 30 days of therapy received at the time of their initial PSR platform
enrollment
Exclusion Criteria:
- Patient who is, or is expected to be inaccessible for follow-up
- Patient with exclusion criteria required by local law
- Patient is currently enrolled in or plans to enroll in any concurrent drug and/or
device study that may confound results
We found this trial at
94
sites
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