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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05066256
Other study ID # Si 752/2020
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 22, 2021
Est. completion date September 2024

Study information

Verified date September 2021
Source Mahidol University
Contact Surat Tongyoo
Phone 6624198534
Email surat.ton@mahidol.ac.th
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Fluid responsive is defined as increasing in Cardiac output or Stroke volume by 10-15% after fluid challenge. Left ventricular diastolic dysfunction is associated with lower left ventricular end-diastolic volume (LVEDV) resulting in a less cardiac output increment after fluid challenge. However, Left ventricular diastolic function indicated by the Mitral E/e' ratio from transthoracic echocardiography, was rarely studied for fluid responsiveness evaluation.


Description:

Fluid therapy is one of the main treatments in patients with shock to increase Oxygen delivery by increasing Cardiac output or Stroke volume. However excess fluid intake may cause fluid overload, resulting in tissue edema, lung edema and organ dysfunction, which can lead to patient deterioration. Fluid responsiveness, defined as increasing in Cardiac output or Stroke volume by 10-15% after fluid challenge, is being recommended to evaluate in-patients with shock, according to European Society of Intensive Care Medicine (ESICM). Cardiac output measurement is often invasive or requires an expensive device, therefore, tests for predicting fluid responsiveness have been used to substitute direct Cardiac output measurement. Left ventricular diastolic dysfunction is associated with a decreasing Left ventricular end-diastolic volume, resulting in a less cardiac output increment after fluid challenge and can be measured by using Mitral E/e' ratio via transthoracic echocardiography. Despite being a non-invasive test, the Mitral E/e' ratio obtained from Echocardiography was rarely studied for the prediction of fluid responsiveness.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age more than 18 years - Diagnosis of shock defined by systolic blood pressure < 90 mmHg or mean arterial blood pressure < 65 mmHg and/or clinical hypoperfusion - Mechanically ventilated without ventilator dyssynchrony and no ventilator triggering - Present of central venous cather or arterial catheter Exclusion Criteria: - Age < 18 years - Frankly hypovolemic shock or hemorrhagic shock - Suspicious of cardiogenic shock - Suspicious of acute decompensated heart failure - Suspicious of acute coronary syndrome - Denied participation or denied inform consent

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Left ventricular diastolic function
Transthoracic echocardiography Mitral E/e'
Inferior vena cava variation
Inferior vena cava variation from ultrasound

Locations

Country Name City State
Thailand Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fluid responsiveness Fluid responsiveness defined by increase in cardiac output at least 15% or increase in systolic blood pressure at least 10 mmHg or increase in mean arterial pressure at least 5 mmHg. 6 hours
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