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Application and Promotion of Pulse-induced Contour Cardiac Output (PiCCO) in Multi-disciplinary Treatment of Heart Failure

Application and Promotion of Pulse-induced Contour Cardiac Output (PiCCO) in Multi-disciplinary Treatment of Heart Failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOC-16009923
Enrollment
Unknown
Registered
2016-11-19
Start date
2016-12-01
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

Heart Failure

Interventions

PiCCO-directed treatment group:treatment directed by conventional monitor combined with PiCCO monitor
Conventional treatment group:treatment directed by conventional monitor

Sponsors

Shanghai Chest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Patients with heart failure of different causes, especially those who need fluid-management or those who are accompanied with other complicated diseases. For example, heart failure accompanied with unstable haemodynamics, cardiorenal syndrome, or cardiogenic liver damage, which is caused by ischemic cardiomyopathy, other kinds of cardiomyopathy, or myocarditis; 2. Patients with heart failure who need hemodynamic monitoring in order to make differential diagnosis; 3. Sever cases who need to be monitored, in order to guide application of vasoactive agents and fluid-management, such as those who are with acute cardiac failure, ARDS, pulmonary arterial hypertension, and hypertensive emergencies; 4. More than 18 years old; 5. Agree to sign a informed consent form; 6. Agree to comply with the research programme.

Exclusion criteria

Exclusion criteria: 1. Patients who are not appropriate for intravascular catheter placement, such as those with peripheral vascular diseases, artery transplantation, puncture site infection, blood coagulation disorders, allergy to heparin; 2. anatomical or physiological derangements likely to render PiCCO-derived measurements grossly inaccurate, such as arrhythmia (e.g. atrial fibrillation), mechanical circulatory assist devices (e.g. IABP, extracorporeal circulation), aortic valve pathology, sever valvular regurgitation, intracardial shunt (e.g. ASD, VSD), sever pneumothorax, lobectomy surgery, massive pulmonary embolism; 3. Pregnant or lactating women; 4. Psychopath; 5. Patients who are taking other experimental drugs; 6. Non-cooperative patients and patients who did not sign informed consent.

Design outcomes

Primary

MeasureTime frame
Mortality rate;rehospitalization rate;time from hospital discharge to rehospitalization;length of hospital stay;hospitalization expense;6-MWD;QOL;BNP;LVEF;size of all chambers of the heart;adverse event rate;

Countries

China

Contacts

Public ContactMin Zhang

Shanghai Chest Hospital

zhangminxk@126.com+86 18017320207

Outcome results

None listed

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