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Clinical registration study on the safety of sacubactril valsartan sodium tablets based on real world

Clinical registration study on the safety of sacubactril valsartan sodium tablets based on real world

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082290
Enrollment
Unknown
Registered
2024-03-26
Start date
2024-04-10
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

For chronic heart failure with reduced ejection fraction, for the treatment of essential hypertension

Interventions

Sacubactril valsartan sodium tablets standard dose group:NA

Sponsors

Wenzhou peoples hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. It is clinically suitable for patients with sakubactril valsartan sodium tablets; 2. Obtain the informed consent and signature of the patient or guardian

Exclusion criteria

Exclusion criteria: 1. There are any contraindications or other circumstances that prohibit the use of sarcubatrol valsartan sodium tablets according to the contraindications and precautions listed in the instruction manual approved by Sarcubatrol Valsartan sodium tablets; 2, poor compliance, unable to complete or refuse to complete the interviewer; 3. Patients with mental disorders and other factors affecting compliance; 4, known allergy to the components of this drug; 5. Researchers believe that candidates are not suitable for admission

Design outcomes

Primary

MeasureTime frame
Blood routine;Liver function;Renal function;

Secondary

MeasureTime frame
Adverse event;

Countries

China

Contacts

Public ContactXiaoshu Chen

Wenzhou People's Hospital

40707729@qq.com+86 135 0666 2820

Outcome results

None listed

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