EarlySense Monitoring Device Evaluation on CHF Patients

EarlySense

Status: Withdrawn

Conditions: Congestive Heart Failure

Treatments: Device: EarlySense monitoring device

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT00382746

ES- CI 02

Details and patient eligibility

About

CHF patients will be monitored using EarlySense ES-16 device and will simultaneously fill diaries and log their weight daily. The data collected and analyzed by the ES-16 device will be correlated with the CHF status data.

Sex: All

Ages: 45+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age over 45 years old
• CHF class II or III with LVEF<40%
• Hospitalized at least once for CHF deterioration over previous 12 month period
• Able and willing to cooperate with this trial for at least a 3 month period
• Home close to participating center

Exclusion criteria

• Recent (within 3 month) admission to ICU or CC-ICU due to severe CHF episode requiring artificial ventilation
• Asthma or COPD