Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (TCTR20260723011) titled 'The Effectiveness of Cardiac Output Monitoring Using Bioreactance technology on shock control within 6-Hour in Septic shock Patients in the Emergency Room at Nakornping Hospital' on July 23.
Study Type: Interventional
Study Design:
Randomized
Primary Sponsor: N/A
Condition:
septic shock
Septic shock
Septic shock
Intervention:
Fluid assessment via standard POCUS (RUSH protocol) evaluating Pump, Tank, Pipe to determine shock type and guide fluid (30ml/kg) or vasopressor use,Assessment via Starling monitor. Baseline CO is measured for 1 minutes, followed by a 100ml fluid challenge over 1 minutes. If delta SVI ...