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A retrospective cohort study of the safety and efficacy of sacubitril valsartan at different initiation time in the treatment of heart failure

A retrospective cohort study of the safety and effectiveness of sacubitril valsartan in the treatment of heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200058617
Enrollment
Unknown
Registered
2022-04-12
Start date
2022-04-12
Completion date
Unknown
Last updated
2024-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Interventions

Observation group:Participants who were prescribed with Naive Sacubitril/valsartan
Control group:Participants who were prescribed Sacubitril/valsartan transfered from ACEi/ARB

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Heart failure patients = 18 years old hospitalized in West China Hospital of Sichuan University from July 2020 to March 2022; 2. The diagnosis of heart failure complies with the diagnostic criteria of the 2018 Chinese Guidelines for the Diagnosis and Treatment of Heart Failure; 3. Use ACEI/ARB or ARNI drugs during hospitalization (at least 3 days before discharge); 4. At least one of the following outcome indicators can be obtained during the follow-up period of 3 months after discharge: patient's survival status, admission due to heart failure, cardiac function, cardiac function (NT proBNP), blood pressure, renal function (glomerular filtration rate) and electrolyte (blood potassium concentration).

Exclusion criteria

Exclusion criteria: 1. Patients taking blood pressure raising drugs at the same time; 2. Patients with contraindications to use ACEI/ARB or ARNI; 3. Cases without important effectiveness monitoring indicators (NT proBNP) and cases without important safety indicators (blood pressure, electrolyte, blood creatinine) before, after and during the 3-month follow-up period.

Design outcomes

Primary

MeasureTime frame
Mortality;Readmission rate of HF;NT-proBNP;

Countries

China

Contacts

Public ContactLuo Min

West China Hospital of Sichuan Universty

luomin200703@126.com+86 28 85422965

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026