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Clinical Trial

CardioMEMS HF System Real-World Evidence Post-Approval Study

NCT: NCT06306573 · ENROLLING_BY_INVITATION

NCT IDNCT06306573
StatusENROLLING_BY_INVITATION
Start Date2022-12-15
Completion2029-12-31
SponsorAbbott Medical Devices (INDUSTRY)
First posted
Last updated

Brief 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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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