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Clinical Trial Summary

Comparison of changes in diastolic pulmonary artery pressure as measured by CardioMEMS™ to impedance parameters as measured by ImpediMed's BIS technology.


Clinical Trial Description

This is a prospective, single-arm, observational, non-randomized clinical study that will enroll patients with heart failure who have had a CardioMEMS™ device implanted to monitor their diastolic pulmonary artery pressure. The study will recruit and enroll ten participants from the Scripps Clinic. Participants will be monitored 3 times a week for a period of 4 weeks. At each monitoring visit, the patient's diastolic pulmonary artery pressure will be measured by CardioMEMS™ and the ImpediMed's BIS technology. Participant's vital signs and weight will also be taken at each monitoring visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02857231
Study type Observational
Source ImpediMed Limited
Contact
Status Completed
Phase
Start date August 7, 2017
Completion date October 9, 2018

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 NCT01162707 - Wireless, Intermittent Monitoring of Right Heart Pressures in HF N/A
Completed NCT02939053 - Correlation of SOZO BIS Measures With CardioMEMS PA Pressure