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Starting soon Observational

Estimating Fluid Requirement in Shocked Traumatic Patients by US on SCV

NCT06726668 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-03-01
Last updated
2024-12-10

Condition(s) studied

ShockTrauma

Study summary

Research question Is the ultrasonographic SCV collapsability index effective in estimating fluid requirements in shocked traumatic Patients ?

Purpose of the study To evaluate the effectiveness of ultrasonograghic SCV collapsibility index before and after the first hour of resuscitation in estimating the First 24 h of fluid requirement in shocked traumatic patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * Traumatic patients who will come to emergency department at Assiut university Hospital between march 2025 to march 2026 and will be admitted after stabilization to the Inpatient ward or ICU Exclusion Criteria: * Patients or their Relatives refuse participation in the study. * Patients who will be transferred to another hospital * • Pregnant women. * Age below 18 and more than 60. * Failure of follow-up of any patient. * Cardiopulmonary resuscitation on arrival. * Contraindicating fluid challenges, such as cardiac insufficiency and Renal failure .

Primary outcome measure(s)

  • To estimate and predict the fluid requirement using ultrasonograghic Sub Clavian vein collapsibility index before and after the first hour of resuscitation — Before resuscitation and after 1 hour of resuscitation
    In the first hour of resuscitation, the patients (unstable shocked) will be given 1 L of crystalloid solution for fluid resuscitation ( according to recent ATLS guidelines). If the patient is still unstable after 1 Liter of fluid or had ongoing blood loss, O- negative blood transfusion will be administered and type-specific blood Will be ordered and the trauma team activated massive transfusion protocol according to recent ATLS Guidelines even if normal hemoglobin. The traumatic patients after 1 h of resuscitation were divided into two groups (SCV non -Repleted) and (SCV Repleted) group as (if thereis still an SCV diameter of \< 7 mm after the first hour of resuscitation they are called (the SCV non -Repleted) group. And if the SCV diameter of ≥ 7 mm after the first hour of resuscitation) they are called the (SCV Repleted) group.

Trial sites (1)

FacilityCityRegionStatus
Assiut University Asyut Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06726668 on ClinicalTrials.gov ↗ ← All trials in Egypt