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Prediction of Fluid Responsiveness in Paediatric Patients With Septic Shock Using Carotid Doppler Ultrasonography and Echocardiography

A

Ain Shams University

Status

Enrolling

Conditions

Echocardiography Guided Fluid Management
Septic Shock

Treatments

Diagnostic Test: echocardiography

Study type

Observational

Funder types

Other

Identifiers

NCT07136532
MD07/2024/2025

Details and patient eligibility

About

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.

Full description

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)

Enrollment

50 estimated patients

Sex

All

Ages

1 month to 16 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

  • Children aged 1 month to 16 years.

  • Patients with septic shock admitted at the PICU during their fluid resuscitative phase were included.Septic shock was diagnosed according to phoenix sepsis score 2024

    • Exclusion criteria:

  • Acquired and congenital heart disease.

  • Acquired and congenital renal disease.

  • Vascular anomalies (e.g. arteriovenous malformation, aneurysm).

  • Suspected intracranial hypertension.

  • Skin lesions or bandages at the sites of ultrasound or echo-cardiography examinations.

  • Anatomical anomalies of the neck.

Trial design

50 participants in 1 patient group

pediatric patients with septic shock
Description:
All patients admitted at Paediatric Intensive care unit (PICU) during the period of the study and met the inclusion criteria. * Sex: Both males and females. * Age: 1 month to 16 years. * Sample size: 50 patients with septic shock admitted at PICU. 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 • Investigations: A) Laboratory: * Complete blood count. * Venous blood gases. * C-reactive protein. * Kidney function tests. * Albumin. * Serum lactate. -Echocardiography (measurement of stroke volume, stroke volume index,cardiac index) _carotid doppler ultrasonography
Treatment:
Diagnostic Test: echocardiography

Trial contacts and locations

1

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Central trial contact

Sara sobhy selim, assistant lecturer

Data sourced from clinicaltrials.gov

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