跳至主要内容
临床试验/NCT04129073
NCT04129073尚未招募不适用

QUO VADIS - QUality Of Life and surviVAl in carDIac arreSt Patients

Gruppo Italiano per la Valutazione degli Interventi in Terapia Intensiva0 个研究点目标入组 1,600 人开始时间: 2022年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,600
主要终点
Neurological Outcome

研究概览

简要总结

QUO VADIS is a national observational study with the aim to describe clinical intervention and utilization of neuroprognostication tools in the management of patients admitted to ICU following cardiac arrest

详细描述

Despite recent improvements in post-resuscitation care, about 50% of patients resuscitated from cardiac arrest die or have poor neurological prognosis. Post-anoxic brain injury is common after cardiac arrest and is a major cause of post-resuscitation mortality. Since there has been a significant investment in improving the emergency response to both in-hospital ad out-of-hospital cardiac arrest (IHCA and OHCA, respectevly) patients and reported improvements in short-term survival outcomes, the long-term neurological state and quality of life of survivors and their caregiver is of growing significance.

QUO VADIS is a national observational study created to describe clinical interventions and utilization of neuroprognostication tools in the management of patients admitted to ICU following cardiac arrest.

The aims of the study are:

  • To create an Italian Registry that describes clinical interventions and neuroprognostication tools used in the management of patients admitted to ICU following cardiac arrest
  • To evaluate, after one year from the cardiac arrest, the neurological outcome and the quality of life of the patients;
  • To evaluate, after one year from the cardiac arrest, the quality of life of caregivers;
  • To identify the most effective clinical intervention in the management of post-cardiac arrest patients admitted to ICU;
  • To create a prognostic model for patients admitted to ICU after cardiac arrest.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
14 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age ≥ 14 years;
  • •Cardiac Arrest within 24 hours ICU admission

排除标准

  • •Absence of Informed consent;
  • •Age < 14 years

结局指标

主要结局

Neurological Outcome

时间窗: 6 months

mRS (modified Ranking Scale) Minimum value: 0 = Complete recovery; Maximum value: 6 = Death

Patients quality of life

时间窗: 12 months

EuroQoL-5D (european quality of life 5 dimensions). 0 = Worst imaginable health state; 100 = best imaginable health state

Disability

时间窗: 6 months

GOSe (Glascow Outcome Scale extended). Minimum value: 1 = Dead; Maximum value: 8= Upper Good Recovery

次要结局

  • Caregiver quality of life(12 months)

研究者

发起方
Gruppo Italiano per la Valutazione degli Interventi in Terapia Intensiva
申办方类型
Other
责任方
Sponsor

相似试验