About this trial
This prospective observational study aims to evaluate the ability of tissue perfusion pressure (TPP) to predict fluid responsiveness in critically ill patients with shock and tissue hypoperfusion. Eligible patients requiring fluid resuscitation will undergo a standardized fluid challenge test. Hemodynamic parameters, including cardiac output and TPP, will be recorded before and after fluid administration. Fluid responsiveness will be defined according to the change in cardiac output following fluid loading. The study will assess the correlation between changes in TPP and cardiac output and evaluate the diagnostic performance of TPP for predicting fluid responsiveness. The results may support the use of TPP as a practical and physiologically relevant parameter for individualized fluid management in patients with shock.
Eligibility criteria
Qualifiers
Age ≥18 years
Admitted to the Intensive Care Unit (ICU)
Diagnosed with shock and evidence of tissue hypoperfusion
Judged by the treating physician to require fluid resuscitation
Disqualifiers
Pregnancy
Immediate requirement for extracorporeal life support, including: VV-ECMO, VA-ECMO, Ventricular assist devices
Expected survival less than 72 hours
Absence of invasive arterial pressure monitoring or arterial waveform availability <25%
Trial design
Treatments tested in this trial
- When the attending physician determines that fluid resuscitation is clinically indicated: Patients will remain in the supine position. Crystalloid solution will be administered intravenously via centr
Treatment groups
Locations
Sponsors and collaborators
Jingyuan,Xu
Lead sponsor
Southeast University, China
Sponsor institution