Heart Failure Therapy and Outcomes in Patients With Heart Failure With Mildly Reduced or Preserved Ejection Fraction
Completed
Conditions studied: Heart Failure With Reduced Ejection Fraction, Heart Failure With Preserved Ejection Fraction
In brief
This was a retrospective observational cohort study using patient data from the Get With The Guideline-Heart Failure (GWTG-HF) registry linked to Medicare Fee-for-Service (FFS) claims. The main goal of the study was to compare home-time in Medicare FFS patients with heart failure with mildly reduced or preserved ejection fraction discharged with sacubitril/valsartan versus those discharged without sacubitril/valsartan.
Key facts
- Study ID
- NCT06671314
- Run by
- Novartis
- People needed
- 42494
- Starts
- 2022-06-02
- Expected to finish
- 2022-10-31
- Last updated by the study team
- 2024-11-04
Who can join
Age: 65 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Hospitalized for heart failure from 01 January 2016 to 30 September 2021.
- Were discharged alive (any discharge disposition other than "Expired").
- Had Mildly reduced or preserved ejection fraction (41% to 60%).
- Had non-missing record of SAC/VAL use at discharge.
- Continuously enrolled in Medicare Part A \& B for the 12 months following the index HF hospitalization discharge date or until death.
You may not qualify if…
- Patients who left against medical advice (AMA), were transferred to an acute care facility, or discharged to hospice care.
- Patients who had dialysis as an in-hospital procedure.
- Patients with a medical history of chronic dialysis.
- Patients with an in-hospital procedure of heart transplantation.
- Patients with a medical history of heart transplantation.
- Patients with an in-hospital procedure of left ventricular assist device.
- Patients with a medical history of left ventricular assist device.
Where it is running
- Novartis Pharmaceuticals — East Hanover, New Jersey, United States
Full record on ClinicalTrials.gov
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