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Personalized CRT - PSR
Recruiting
I'm InterestedTrial ID: NCT03723265
Purpose
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.
Official Title
Personalized CRT - Product Surveillance Registry (PSR)
Eligibility
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
Intervention(s):
device: Cardiac Resynchronization Therapy
Recruiting
I'm InterestedContact Information
Stanford University
School of Medicine
300 Pasteur Drive
Stanford,
CA
94305