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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05888974
Other study ID # 2023-A00022-43
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 1, 2023
Est. completion date December 31, 2024

Study information

Verified date June 2023
Source Centre Hospitalier Universitaire de Nimes
Contact Laura GRAU MERCIER, MD
Phone +33675169725
Email laura.merciergr@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Assessing the response to vascular filling in shock is a challenge in emergency medicine. The mitral annulus velocity measured by tissue Doppler (E') has recently been characterized as sensitive to the preload conditions of a patient. The investigators hypothesize that the E' variation (∆E') before and after fluid filling allows us to assess the response to vascular filling. The investigators hypothesize that the ∆E' has a good diagnostic performance to establish whether a patient is responsive to fluid filling, defined by an area under the ROC curve greater than 0.75.


Description:

Assessing the response to vascular filling in shock is a challenge in emergency medicine. Trans thoracic ultrasound (TTS) is recommended for the diagnosis and management of this type of patient. TTS allows real-time monitoring of the effectiveness of a therapeutic . In case of circulatory failure without cardiac failure, it is recommended to perform fluid filling tests based on an increase in of indicators to assess preload dependence. The change in subaortic VTI, which has become the gold standard in clinical practice for diagnosing fluid filling response, suffers from a lack of technical feasibility. The mitral annulus velocity measured by tissue Doppler (E') has recently been characterized as sensitive to the preload conditions of a patient. The high feasibility of this technique makes its study interesting for the evaluation of the preload (and its variation after variation after vascular filling) of the patient in shock in the emergency department. To our knowledge, there are no clinical studies exploring the relevance of this technique to evaluate fluid filling response in patient admitted with shock in the emergency department. The investigators hypothesize that the E' variation (∆E') before and after fluid filling allows us to assess the response to vascular filling. The investigators hypothesize that the ∆E' has a good diagnostic performance to establish whether a patient is responsive to fluid filling, defined by an area under the ROC curve greater than 0.75. The main objective of this study is to investigate the diagnostic performance of ∆E' in establishing response to fluid filling in a prospective cohort of patients admitted to the emergency department with shock requiring vascular filling.


Recruitment information / eligibility

Status Recruiting
Enrollment 187
Est. completion date December 31, 2024
Est. primary completion date July 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient has been informed of the study and does not refuse to participate. - Patient is at least = 18 years of age. - The patient must be beneficiary of a health insurance plan. - Patient has shock with a mean blood pressure less than 65 mmHg (<) - The patient does not have acute intracranial pathology - The referring physician has decided on a vascular filling with 500mL of crystalloids (NaCl 0.9% or Ringer lactate) Exclusion Criteria: - The patient has already received 2 vascular fillings since the beginning of his management - The patient is in shock and has a contraindication to vascular filling : shock of a cardiogenic or obstructive nature - The patient has an intracranial pathology requiring maintain a MAP = 80 mmHg - The patient is intubated or on Non-Invasive Ventilation before the vascular filling - The patient is under court protection - The patient is pregnant, parturient or nursing

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Cardiac ultrasonography
During the inclusion visit, the patient will receive 3 cardiac ultrasonography. The first one will be performed at the time of the initiation of the 500mL vascular filling (T0), without delaying and the second one after the end of the filling (Tfin). These first two ultrasound are part of standard practice. A third will be performed 20 minutes after the end of the vascular filling (Tfin+20).

Locations

Country Name City State
France CHU de Nîmes Nîmes

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nimes

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary E' variation (?E') The E' wave will be measured by tissue Doppler at the initiation (T0) of the filling and after the end of the vascular (Tfin) to determine its variation (%) between these two times of measurement. Inclusion time
Primary Fluid filling responsiveness Vascular filling is defined by the intravenous administration of 500 mL of crystalloid for 20 to 30 minutes, decided by the physician in charge. The response to filling will be evaluated by the variation of the time velocity index between T0 and Tfin (?ITV) measured with pulsed Doppler.
Patients will be considered :
Responder (R) group if ?ITV = 15%
Nonresponder group (NR) if ?ITV < 15%.
Inclusion time
Secondary ?E'late ?E'late: the E' wave will be measured by trans thoracic ultrasound before vascular filling (T0) and 20 minutes after the end of vascular filling (Tfin+20) to determine its variation (%) between these two times of measurement. Inclusion time
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