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Observation study for the application of phosphocreatine injection in patients with heart failure and sarcopenia

Observation study for the application of phosphocreatine injection in patients with heart failure and sarcopenia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032916
Enrollment
Unknown
Registered
2020-05-15
Start date
2020-05-14
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Heart failure

Interventions

Two groups:phosphocreatine versus normal saline

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Patients who voluntarily participate, understand and sign informed consent; 2. NYHA heart function grade II-IV in patients with heart failure diagnosis criteria: (1) Echocardiography has abnormal cardiac structure with abnormal systolic or diastolic function. LVEF does not make specific regulations; (2) Have at least one heart failure symptom and one physical sign or chest radiograph result 3. Heart failure symptoms: (1) Dyspnea occurs when breathing is difficult or slight activity occurs in a resting state; (2) Fatigue; (3) Decreased activity tolerance; 4. Signs of heart failure: (1) Moist rales appeared in lung field; (2) Peripheral edema; (3) Increase of jugular vein pressure or neck vein distention; 5. Patients with pulmonary congestion or edema indicated by chest film; 6. NT-proBNP>=1000pg/ml; 7. Patients who meet the diagnostic criteria for sarcopenia proposed by the Asian Working Group on sarcopenia in 2016.

Exclusion criteria

Exclusion criteria: 1. Patients with different intention; 2. Patients who have poor compliance or are unable to participate in the trial due to serious clinical conditions; 3. Patients with severe liver and kidney function damage; 4. Patients who had undergone major cardio cerebrovascular surgery within 3 months before randomization, or expected to undergo major cardio cerebrovascular surgery within 3 months; 5. Patients who are allergic to sodium creatine phosphate; 6. Patients with other muscle diseases or other diseases affecting physical activity.

Design outcomes

Primary

MeasureTime frame
NT-proBNP;LVEF;Muscle mass;Quantity and quantity of exosome protein;Expression of mitochondrial protein marker in exosomes;Inflammatory factor level;

Countries

China

Contacts

Public ContactYanqiu Xing

Qilu Hospital of Shandong University

xingyanqiu@sina.com+86 18560082269

Outcome results

None listed

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