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Clinical Trial Summary

The purpose of the trial is to evaluate the wireless monitoring of pulmonary artery pressure using the CardioMEMS HF Pressure Measurement System in adult subjects with NYHA Class III Heart Failure.


Clinical Trial Description

The trial is designed to demonstrate that the CardioMEMS Sensor can be positioned in the right or left pulmonary artery, and that Sensor pressure measurements correlate to standardized methods of intra-cardiac pressure measurements post-sensor implant and at the 60 day visit. Safety will be monitored by the occurrence of adverse events throughout the trial. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01162707
Study type Interventional
Source CardioMEMS
Contact
Status Completed
Phase N/A
Start date December 2006
Completion date September 2012

See also
  Status Clinical Trial Phase
Completed NCT01381172 - Evaluate Safety and Efficacy of the OPTIMIZER® System in Subjects With Moderate-to-Severe Heart Failure: FIX-HF-5C N/A
Completed NCT02857231 - Bioimpedance Spectroscopy Compared to CardioMEMS™
Completed NCT02939053 - Correlation of SOZO BIS Measures With CardioMEMS PA Pressure