Actively Recruiting

Age: 18Years - 50Years
All Genders
NCT07550400

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

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

40

Participants Needed

1

Research Sites

27 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Fluid replacement is considered the cornerstone of hemodynamic management in critically ill patients especially in patients with septic shock. However, only about 50% of critically ill hemodynamically unstable patients are responsive to fluids. Consequently, the resuscitation of critically ill patients requires an accurate assessment of the patients' intravascular volume status and their volume responsiveness. In this study, we will compare the efficacy of carotid artery flow to echo left ventricular end diastolic volume as a predictive value for fluid resuscitation in septic shock patients.

CONDITIONS

Official 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 according to 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), heart rate over 120 bpm without other cause, low urine output (<1 ml/kg in last hour), high blood lactate (>2 mmol/l) without other cause, or prolonged 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 stenosis over 50% or previous carotid surgery
  • Contraindications to carotid artery Doppler including wounds, infections, or occlusions of carotid artery
  • Arrhythmias that affect stroke volume assessment such as atrial fibrillation or frequent premature ventricular contractions
  • Dilated cardiomyopathy
  • Poor transthoracic echocardiographic window
  • Patient refusal

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

CONTACT

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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