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Effect of sacubitril valsartan combined with sodium-glucose cotransporter protein 2 inhibitor in the treatment of patients with acute heart failure combined with diuretic resistance and the effect on cardiac function

Effect of sacubitril valsartan combined with sodium-glucose cotransporter protein 2 inhibitor in the treatment of patients with acute heart failure combined with diuretic resistance and the effect on cardiac function

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118845
Enrollment
Unknown
Registered
2026-02-11
Start date
2023-07-31
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

acute heart failure

Interventions

Experimental group:On the basis of the control group, sacubitril valsartan tablets 100mg twice a day (50mg twice a day for patients not taking ARB drugs or taking low-dose ARB drugs and for patients w
Control group:Heart failure comprehensive pharmacotherapy was administered alone, including loop diuretics, ß blockers, mineralocorticoid receptor antagonists (all at identical doses), inotropic agent

Sponsors

Quzhou Kecheng District People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.All patients meet the diagnostic criteria outlined in the "Guidelines for Primary Care Diagnosis and Treatment of Acute Heart Failure (2019 Edition)"; 2.Meet the diagnostic criteria for diuretic resistance: daily intravenous furosemide >= 80 mg, or equivalent daily dose of other diuretics, yet unable to achieve adequate urine output (0.5–1.0 mL/kg/h); 3. Complete baseline information available and participation in all trial procedures; 4. Informed consent obtained.

Exclusion criteria

Exclusion criteria: 1. Patients with cardiogenic shock, severe respiratory diseases with marked hypoxemia and hemodynamic instability, hematologic disorders, autoimmune diseases, severe hepatic or renal disease (eGFR <= 30 mL/min/1.73 m^2), severe arrhythmias, myocarditis, acute myocardial infarction, severe electrolyte disturbances, acid-base imbalance, severe infections, or malignancies; 2. Patients with contraindications to sacubitril/valsartan or SGLT-2 inhibitors; 3.Patients currently taking ACE inhibitors; 4.Patients with psychiatric disorders or communication barriers; 5. Patients with a history of drug allergies; 6.Patients who have participated in other clinical trials within the past two months.

Design outcomes

Primary

MeasureTime frame
24h urine output;Weight;6-minute walk test results;

Secondary

MeasureTime frame
Serum creatinine level;N-terminal pro-B-type Natriuretic Peptide;Diuretic efficiency;Dyspnea score;Changes in the patient's heart function;

Countries

China

Contacts

Public ContactMinglei Zhang

Quzhou Kecheng District People's Hospital

759908684@qq.com+86 570 826 0123

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026