Clinical Trials Directory

Trials / Unknown

UnknownNCT03020043

Evaluation of Longterm Outcome of New York Heart Association Class III Heart Failure Patients Receiving Telemonitoring Using a Pulmonary Artery Pressure Sensor System (CardioMEMS)

CardioMEMS Registry of the Frankfurt Heart Failure Center

Status
Unknown
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Johann Wolfgang Goethe University Hospital · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Invasive hemodynamic monitoring in advanced heart failure patients is a relative new option. In order to investigate the impact of remote telemonitoring of pulmonary artery pressures on mortality and morbidity in a routine clinical setting in Germany, the investigators initiated this multicenbtric registry.

Detailed description

All patients who receive invasive hemodynamic monitoring using a pulmonary artery pressure sensor (CardioMEMS device) are offered participation in the registry. Routine heart-failure parameters, lab values, medication and QoL as obtained on the regular outpatients visits in the department are entered into a registry-specific database. The investigators plan to asses the impact of telemonitoring on mortality, morbidity and QoL as well as on Guideline-recommended heart failure medication. In addition, it is planned to quantify the input in person time for telemonitoring.

Conditions

Timeline

Start date
2016-08-01
Primary completion
2024-12-01
Completion
2025-12-01
First posted
2017-01-13
Last updated
2019-09-18

Locations

2 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT03020043. Inclusion in this directory is not an endorsement.