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Efficacy of strain and synchrony of intermittent repeated levosimendan infusions in chronic heart failure patients

Efficacy of strain and synchrony of intermittent repeated levosimendan infusions in chronic heart failure patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064259
Enrollment
Unknown
Registered
2022-10-01
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

heart failure

Interventions

treatment group:intermittent repeated levosimendan infusions
Conrol group:Optimal drug treatment and capacity management education

Sponsors

Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Older than 18 years old; LVEF < 35%; NYHA cardiac function classification ?-? in recent 3 months; There was no low cardiac output at enrollment; No pulmonary or systemic circulation congestion requiring emergency medical treatment at enrollment; The patient has been treated with the best medication (except for intolerance or contraindications); The patient was informed and signed the informed consent

Exclusion criteria

Exclusion criteria: 1. Left ventricular outflow tract obstruction; 2. Primary valvular disease without surgical correction; 3. Severe ventricular arrhythmias; 4. Acute coronary syndrome within 3 months; 5. Stroke in 3 months; 6. hypertrophic cardiomyopathy or restrictive cardiomyopathy; 7. He had used milrinone, dopamine and dobutamine within 3 days. 8. within 28 days had used levosimendan; 9. Blood potassium < 3.5mmol/L; Creatinine clearance rate < 30ml/min/m2; 10. We plan to implant CRT, ICD, CCM, heart transplant, and left ventricular assist device within one year. 11. Patients are participating in additional clinical trials; 12. Clinical conditions that were considered inappropriate for enrollment by the investigators.

Design outcomes

Primary

MeasureTime frame
Mortality;Cardiovascular death;left ventricular strain and time to peak;

Countries

China Mainland (PRC)

Contacts

Public ContactSuxia Guo

Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital)

Guo7771812@163.com+86 13665103927

Outcome results

None listed

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