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NCT Number: NCT07438301

Septic Shock Hemodynamic Respond to Volume Resuscitation Versus Vasopressor Administration

The goal of this observational study is to learn about the change of hemodynamic response from intravenous fluid versus medical (vasopressor) resuscitation by echocardiogram in septic shock patient.

The main question it aims to answer is:

How hemodynamic response change from intravenous fluid versus medical (vasopressor) resuscitation by echocardiogram in septic shock patient?

Participants already receiving the appropriate resuscitation at that time by their medical staff as part of their regular medical care for septic shock. The echocardiogram will assess before and after resuscitation.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

The goal of this observational study is to learn about the change of hemodynamic response from intravenous fluid versus medical (vasopressor) resuscitation by echocardiogram in septic shock patient.

The investigators enrolled septic shock patients, who required hemodynamic resuscitation. Then the investigators performed baseline echocardiogram to measured stroke volume, cardiac output and E/Ea before start resuscitation. In fluid resuscitation group, patient will received either fluid resuscitation about 200 mL to 500 mL before preformed echo after fluid resuscitation. In vasopressor group, patient will received norepinephrine titration dose about 0.05 mcg/kg/min, before performed echocardiogram. Then the investigators compare the different change between those resuscitation with fluid and with vasopressor titration, in term of stroke volume, cardiac output, cardiac index and E/Ea change.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients aged ≥18 years
  • Diagnosis with Septic Shock (Sepsis-3 Definition of Septic Shock)
  • Hypotension, SBP < 90 mmHg, or mean arterial BP < 65 mmHg

Exclusion criteria

  • Patients who receive two or more vasopressors
  • Patients who receive inotropic medications
  • Patients who receive simultaneously fluid with vasopressor resuscitation
  • Patients with insufficiently quality ultrasound images for determining echocardiography
  • Patients or their legally authorized representatives (LAR), who decline participation in the study or are unable to provide informed consent before enrollment

Treatment and study plan

Echocardiogram

Diagnostic Test

Patient will be undergone echocardiogram for hemodynamic evaluation, before and after resuscitation by fluid and by vasopressor

Primary outcomes

  1. Change in Cardiac Index

    Time frame: T0 = Cardiac index before resuscitation T1= Cardiac index 15minutes after resuscitation by IV fluid or Vasopressor (Post-resuscitation)

    Change of Cardiac Index from pre-to-post resuscitation

    • Cardiac index before resuscitation
    • Cardiac index 15minutes after resuscitation by IV fluid or Vasopressor (Post-resuscitation)

Secondary outcomes

  1. Change of other echocardiographic parameter from baseline to post-resuscitation.

    Time frame: T0 = Echocardiographic parameters before resuscitation T1= Echocardiographic parameters 15minutes after resuscitation by IV fluid or Vasopressor (Post-resuscitation)

    Change in other echocardiographic parameter; IVC variation, Left ventricular ejection fraction, Left ventricular diastolic function in form of E/A ratio and E/E' ratio; from baseline to post-resuscitation;

    Fluid resuscitation vs Vasopressor Resuscitation and its correlation with clinical parameters below

  2. 28-day Mortality

    Time frame: 28 days

    death outcome

Study contacts

Contact information is provided by the study sponsor or research team.

Surat Tongyoo, MD

CONTACT

[email protected]

+66824198534

Sponsors and collaborators

Lead sponsor

Mahidol University

Other

Registry information

Official study title

Echocardiographic Assessment the Different of Septic Shock Resuscitation: Comparison of Volume Expansion Versus Vasopressor Administration

Acronym: ECHO-VEVA

Important dates

Study start
2026
Primary completion
2026
Study completion
2028
First posted
Feb 27, 2026
Registry last updated
Feb 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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