CardioMEMS HF System Post Approval Study
NCT02279888 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1214
Last updated 2024-04-17
Summary
The purpose of the CardioMEMS HF System Post Approval Study (PAS) is to evaluate the use of the CardioMEMS HF System in patients with NYHA class III heart failure in a commercial setting.
Conditions
- Heart Failure
- Left-Sided Heart Failure
- Congestive Heart Failure
Interventions
- DEVICE
-
CardioMEMS HF System
Pulmonary artery pressure sensor
Sponsors & Collaborators
-
Abbott Medical Devices
lead INDUSTRY
Principal Investigators
-
Lynne Stevenson, MD · Brigham and Women's
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-01-31
- Primary Completion
- 2019-10-11
- Completion
- 2019-10-11
Countries
- United States
Study Locations
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