Observational study for Patients with LVAD and a CardioMEMS

Trial ID:
IRB-17-7102
Thomas Heywood, M.D.
This study will collect follow-up data on patients with CardioMEMS and LVAD devices. Participants will have study visits at baseline, 1 month, 3 months and 6 months.

Inclusion Criteria

  • Have a CardioMEMS HF PA Sensor and a commercially-approved HeartMate LVAD
  • Be at least 18 years or older
  • Be able to complete a 6 minute heart walk test

Exclusion Criteria

  • Not be currently participating in any other device study

Additional Info

  • The goal of this study is to see if CardioMEMs and LVAD devices help to improve symptoms and reduce the chance of re-hospitalization for patients with heart failure.

Contact Info:

  • Heather Catchpole
  • catchpole.heather@scrippshealth.org