CardioMEMS HF System Real-World Evidence Post-Approval Study

Status Enrolling by invitation

Clinical Trial Summary

The purpose of this post-approval study (PAS) is to evaluate the long-term safety and effectiveness of the CardioMEMS™ HF System using real-world evidence (RWE) methods.

Clinical Trial Description

Subjects will be identified in Abbott's Merlin.net remote monitoring database. Merlin.net data will be linked to Medicare fee-for-service (FFS) claims data to longitudinally track outcomes. Each subject will be followed for a minimum of 36 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06306573
Study type	Observational
Source	Abbott Medical Devices
Contact
Status	Enrolling by invitation
Phase
Start date	December 15, 2022
Completion date	December 31, 2028

View Details

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