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Evaluating the efficacy of creatine phosphate, levosimendan and Recombinant Human Brain Natriuretic Peptideon on chronic heart failure using blood levels of Galectin-3, Copeptine, ST-2, and NT-proBNP

Evaluating the efficacy of creatine phosphate, levosimendan and Recombinant Human Brain Natriuretic Peptideon on chronic heart failure using blood levels of Galectin-3, Copeptine, ST-2, and NT-proBNP

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15006512
Enrollment
Unknown
Registered
2015-05-10
Start date
2015-06-05
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

chronic heart failure

Interventions

conventional treatment group:Heart failure (routine therapy including positive inotropic drugs, diuretics and vasodilator, angiotensin converting enzyme inhibitors, beta-blockers, phosphodiesterase in
phosphocreatine group:On the basis of routine therapy heart failure combined with creatine phosphate
Levosimendan group:On the basis of routine therapy heart failure combined with Levosimendan
Recombinant Human Brain Natriuretic Peptideon group:On the basis of routine therapy heart failure combined with Recombinant Human Brain Natriuretic Peptideon

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. cardiac insufficiency symptoms or signs; 2. heart function in line with the New York heart association class III-IV; 3. the hospital inpatients; 4. use our echocardiography, confirmed that the left ventricular ejection fraction (LVEF) of 40% or less; 5. all the subjects or his guardian consent form must be signed before entering the test subjects.

Exclusion criteria

Exclusion criteria: 1. acute myocardial infarction, or other causes of acute left heart failure; 2. with pure severe valvular stenosis (aortic and mitral valve), hypertrophic or restrictive cardiomyopathy; 3. serious ventricular arrhythmia; 4. the test drug allergy or taboo; 5. uncontrolled thyroid disease; 6. decubitus systolic blood pressure 180 mmHg; 7. liver and kidney function is not completed; 8. cardiac shock, blood volume is insufficient or cannot use vasodilator; 9. participated in other clinical researchers within three months.

Design outcomes

Primary

MeasureTime frame
Galectin-3;Copeptine;ST2;NT-prpBNP;

Countries

China

Contacts

Public ContactXing Yanqiu
xingyanqiu@sina.com+86 18560082269

Outcome results

None listed

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