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Withdrawal of Neprilysin Inhibition for heart failure in ARNI responders with recovered ischemic cardiomyopathy

Withdrawal of Neprilysin Inhibition for heart failure in ARNI responders with recovered ischemic cardiomyopathy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900028191
Enrollment
Unknown
Registered
2019-12-15
Start date
2020-03-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

ischemic heart disease

Interventions

ARNI :continous administration ARNI
ARNI stopped:stop ARNI, only taking Valsartan

Sponsors

Changzhou 2nd Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. dilated cardiomyopathy with LVEF 40% or lower, absence of current symptoms of heart failure; 2. aged more than 18 years; 3. administration of sacubitril/valsartan(LCZ696) more than 3 months, and LVEF more than 50% after totally revascularization; 4. all of the patients are informed consent.

Exclusion criteria

Exclusion criteria: 1. pregnancy; 2. estimated glomerular filtration rate less than 30ml/min/1.73m2; 3. severe liver failure; 4. angioedema; 5. moderate or severe valvular heart disease.

Design outcomes

Primary

MeasureTime frame
the relapse of heart failure;NT-pro-BNP;

Secondary

MeasureTime frame
the remolding measurements by echocardiology;KCCQ scores;Blood potassium;renal function;

Countries

China

Contacts

Public ContactYuanJi

Changzhou 2nd Hospital

jiyuan1213@aliyun.com+86 13196788055

Outcome results

None listed

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