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A single-center, randomized, double-blind clinical study for Zhenwu decoction in the treatment of cardiorenal syndrome

A single-center, randomized, double-blind clinical study for Zhenwu decoction in the treatment of cardiorenal syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022487
Enrollment
Unknown
Registered
2019-04-13
Start date
2019-04-17
Completion date
Unknown
Last updated
2019-04-15

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

Conditions

cardiorenal syndrome

Interventions

1:zhenwutang decotion
2:placbo

Sponsors

Zhujiang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) aged 18-85 years, male or female; (2) accord with the diagnostic criteria of chronic heart failure, and have a history of chronic heart failure of more than 3 months or clinical symptoms of heart failure for more than 3 months; (3) color doppler echocardiography showed that left ventricular ejection fraction (LVEF) was less than 50% (modified Simpson method); (4) NYHA cardiac function classification ? ~ IV (hemodynamic stability and no need for intravenous administration); (5) the content of serum NT-proBNP was = 450 PG = ml; (6) those who received standardized drug treatment for at least 2 weeks without adjusting the dosage and intravenous therapy.

Exclusion criteria

Exclusion criteria: (1) patients scheduled for coronary artery revascularization within 12 weeks, cardiac resynchronization therapy or cardiac resynchronization therapy within 12 weeks; (2) patients with tumor, severe neuroendocrine system diseases and psychosis; (3) patients with left ventricular outflow tract obstruction, myocarditis, hypertrophic cardiomyopathy, restrictive cardiomyopathy, large aneurysms, arterial dissection, congenital heart disease and unrepaired hemodynamic changes; (4) uncontrolled hypertensive patients with systolic blood pressure = 180/mmHg and / or diastolic blood pressure = 110 mmHg; (5) pregnant or preparing for pregnancy and lactation; (6) allergic constitution, or those who are known to be allergic to therapeutic drugs; (7) patients preparing for renal replacement therapy in the near future; (8) 1 months to participate in other drug clinical researchers; (9) According to the researcher's judgment, the patient was unable to complete the study or was unable to comply with the requirements of the study (for managerial or other reasons).

Design outcomes

Primary

MeasureTime frame
NT-proBNP;Creatinine;

Countries

China

Contacts

Public ContactFu Qiang

Zhujiang Hospital, Southern Medical University

fuqiang020@126.com+86 18680288708

Outcome results

None listed

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