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The goal of this study is to evaluate the role of carotid Doppler and Echocardiography as a predictor of fluid responsiveness in paediatric patients with septic shock. and To evaluate the diagnostic accuracy of Aortic peak velocity and velocity time integral (VTI)variation in patients with septic shock during their fluid resuscitation phase as a reliable predictor of fluid responsiveness.
The goal of this study is to evaluate the role of carotid Doppler and Echocardiography as a predictor of fluid responsiveness in paediatric patients with septic shock. and To evaluate the diagnostic accuracy of Aortic peak velocity and VTI variation in patients with septic shock during their fluid resuscitation phase as a reliable predictor of fluid responsiveness.All patients included in the study will be evaluated clinically and radiologically at fluid resuscitative phase of septic shock after fluid resuscitation. This evaluation will include: • Clinical examination: Clinical evaluation will be done initially and after fluid resuscitation: * Vital data (systolic, diastolic, and mean blood pressure, heart rate, Temperature). * Urine output, capillary perfusion time, Central venous pressure (CVP). * Detailed physical examination (chest, heart, and abdomen). • Investigations: A) Laboratory: * Complete blood count. * Venous blood gases. * C-reactive protein. * Kidney function tests. * Albumin. * Serum lactate. * Fibrinogen * Serum electrolytes. * Fibrinogen to albumin ratio B) Imaging: Echocardiography (measurement of stroke volume, stroke volume index, cardiac index, systemic vascular resistance index, Aortic peak velocity and VTI variation,, inferior vena cava (IVC)collapsibility index and IVC distensibility index)
Age
0 - 16 years
Sex
ALL
Healthy Volunteers
Yes
Ain shams university _faculty of medicine
Cairo, Egypt
Start Date
September 1, 2025
Primary Completion Date
September 1, 2026
Completion Date
March 1, 2027
Last Updated
August 22, 2025
50
ESTIMATED participants
echocardiography
DIAGNOSTIC_TEST
Lead Sponsor
Ain Shams University
NCT07179276
NCT07383103
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT07388628