Actively Recruiting

Age: 18Years - 50Years
All Genders
ID07550400

Echocardiographic Left Ventricular End Diastolic Area Versus Carotid Artery Duplex as Indicators for Guiding Fluid Resuscitation in Septic Shock Patients

Led by Ain Shams University · Updated on 2026-04-24

40

Participants Needed

1

Research Sites

1 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating methods to guide fluid resuscitation in critically ill patients with septic shock, a condition where blood flow is dangerously low. This study focuses on comparing carotid artery flow measurements with echocardiographic left ventricular end diastolic volume to predict which patients will respond to fluid treatment. Only about half of critically ill patients with unstable circulation respond to fluids, so accurate assessment tools are needed to improve care. The study involves two main procedures performed within 1 to 2 hours of ICU admission: carotid artery duplex ultrasound and echocardiography to measure left ventricular end diastolic area (LVEDA). Patients receive fluid resuscitation following guidelines, with 30 ml/kg of IV crystalloid fluid given as 500 ml boluses over 15 minutes. A fluid challenge of 1000 ml Ringer acetate solution is then rapidly infused over 30 minutes. The ultrasound and echocardiography measurements are repeated after fluid infusion to see if blood flow or heart chamber size changes indicate fluid responsiveness. Participants will be monitored closely in the ICU, with ultrasound and echocardiographic assessments before and after fluid treatment. Researchers will measure the accuracy of these imaging tools within one day to predict fluid responsiveness. The study also records clinical signs of circulatory failure. Data will be collected to evaluate the effectiveness of these noninvasive techniques for guiding fluid management in septic shock patients. The total study participation duration varies depending on ICU admission and monitoring needs.

CONDITIONS

Brief Title

Role of Echocardiography and Ultrasound Indices in Resuscitation of Septic Shock Patients

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 50 years old
  • Both males and females
  • Diagnosed with septic shock with a SOFA score of 1 or higher
  • Presence of at least one sign of acute circulatory failure such as low blood pressure (mean arterial pressure <65 mmHg or systolic <90 mmHg)
  • Tachycardia over 120 bpm without other obvious cause
  • Oliguria less than 1 ml/kg in the last hour suggestive of circulatory failure
  • Blood lactate level over 2 mmol/l without other known cause
  • Other signs of circulatory failure like increased capillary refill time over 2 seconds
Not Eligible

You will not qualify if you...

  • Known significant valvular heart disease such as severe aortic insufficiency or stenosis
  • Known carotid artery narrowing greater than 50% or previous carotid surgery
  • Contraindication to carotid artery Doppler including wound, infection, or carotid artery occlusion
  • Heart rhythm problems affecting stroke volume assessment like atrial fibrillation or frequent premature ventricular contractions
  • Dilated cardiomyopathy
  • Poor echocardiographic window preventing clear imaging
  • Patient refusal to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Within the first 3 hours of ICU admission

Participants undergo carotid artery duplex and echocardiography assessments to evaluate fluid responsiveness during septic shock resuscitation.

1 to 2 visits within 3 hours of ICU admission

Trial Site Locations

Total: 1 location

1

Faculty of medicine, Ain Shams University

Cairo, Egypt

Actively Recruiting

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Research Team

B

baheya kamel

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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