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Critical Care Ultrasound Oriented Shock Treatment in ICU

Not Applicable
Completed
Conditions
Shock
Interventions
Other: Critical care ultrasound
Registration Number
NCT03093987
Lead Sponsor
West China Hospital
Brief Summary

Objective

To investigate whether critical care ultrasound oriented shock management in shock patients in intensive care unit(ICU) can improve outcome.

Methods

Randomized controlled research. Patients were randomly allocated to two groups. In the critical care ultrasound oriented shock management group (CUSS group), treatment was oriented by the findings of critical care ultrasound in each shock phase, while in the control group the decisions about the monitoring and management were made by the clinical team. The goal of treatments in both groups were decreasing lactate by 20% or more per 2 hours for the Optimization phase in shock management, and no increase lactate level when removing the fluid in de-escalation phase. The primary outcome measure were hospital mortality and 28-day mortality, the secondary outcome measure were the length of ventilation and the length of ICU stay.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
150
Inclusion Criteria
  • SBP <90 mm Hg or MAP <65 mm Hg or SBP decrease >40mmHg or need vasoactive drugs;
  • Skin that is cold and clammy,capillary refill time >4.5s,urine output of<0.5ml/Kg.hr and lactate >2mmol/L;
  • SHOCK presented within 6 hr.
Exclusion Criteria
  • <18 years old;
  • Pregnancy;
  • Patient or family member refuse to be enrolled.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
critical care ultrasoundCritical care ultrasoundCirculation management will be adjusted according to the results of critical ultrasound combined with clearance of lactic acid in patients with shock.
Primary Outcome Measures
NameTimeMethod
28-day mortalitythrough study completion,an average of 28 days

28-day mortality

Secondary Outcome Measures
NameTimeMethod
the incidence of AKIthrough study completion,an average of 28 days

the incidence of AKI

the total length of hospital staythrough study completion,an average of 28 days

the total length of hospital stay

the length of ICU staythrough study completion,an average of 28 days

the length of ICU stay

Trial Locations

Locations (1)

West China Hospital of Sichuan University

🇨🇳

Chengdu, Sichuan, China

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