Health Condition 1: I509- Heart failure, unspecified
Conditions
Interventions
Intervention1: Abbott Sensor Based Monitoring System: The study intervention device would require the implantation of sensor-based system in Chronic Heart Failure patients for a total participation of
Sponsors
Abbott Healthcare Pvt Ltd
Eligibility
Inclusion criteria
Inclusion criteria: At least 18 years of age with diagnosis of heart failure
Exclusion criteria
Exclusion criteria: Subject has known concomitant medical condition, in which, in the opinion of the investigator could present risk to the subject. Subject is currently participating in another interventional clinical trial For female participants, subject must not be pregnant or planning to become pregnant during the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Study the feasibility of sensor-based monitoring device in ambulatory patients with chronic heart failure.Timepoint: 90 Days | — |
Secondary
| Measure | Time frame |
|---|---|
| All cause readmissions Recurrent heart failure hospitalizations (HFH) or emergency department or hospital outpatient observation visits for intravenous diuretic therapy Six-Minute Hall Walk test at baseline & study completion NYHA assessment from baseline to study exit.Timepoint: 90 Days | — |
Countries
India
Contacts
Public ContactSumit Anand
Abbott India Pvt. Ltd
Outcome results
None listed