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Real World Experience in Heart Failure With Reduced Ejection Fraction (HFrEF) Patients Treated With sAc/vaL.

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Novartis

Status

Completed

Conditions

Heart Failure

Treatments

Drug: Sacubitril/Valsartan

Study type

Observational

Funder types

Industry

Identifiers

NCT05448872
CLCZ696BIT08

Details and patient eligibility

About

The study is a cohort observational, retrospective, non-interventional study.

Full description

Study period:

Index date: The index date were defined as the first date of the first prescription of Sacubitril/Valsartan during inclusion period and this were used to establish the beginning of the follow-up period.

Characterization period: 6 months period before the index date were used to characterize patients.

Follow-up period: Any patients has at least 1 year of follow-up. Follow-up period went from index date to June 2020.

Enrollment

924 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Consecutive ambulatory patients with a diagnosis of HF that attended the Outpatient Clinics for HF management and who have been prescribed Sacubitril/Valsartan from 01 October 2016 to 30 June 2019 (inclusion period) were included in the study. To allow for at least 1-year follow-up period for any patients, the observation period ended by 30 June 2020.

In detail, all patients attending by outpatient clinics for the diagnosis and treatment of HF in the Italian Centers involved, with:

  • age ≥18 years old AND
  • at least one prescription of Sacubitril/Valsartan from 01 October 2016 to 30 June 2019 were included in the study.

Exclusion criteria

  • Missing age or sex information.

Trial design

924 participants in 1 patient group

Sacubitril/Valsartan
Description:
Heart Failure (HF) patients treated with Sac/Val
Treatment:
Drug: Sacubitril/Valsartan

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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