跳至主要内容
临床试验/NCT05326789
NCT05326789Unknown不适用

Coronary and Cerebral Perfusion Optimization in Cardiac Arrest: A Feasibility and Physiological Study

Ciusss de L'Est de l'Île de Montréal0 个研究点目标入组 20 人开始时间: 2022年5月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
20
主要终点
success rate and time of REBOA inflation during non-traumatic arrest in a community hospital

研究概览

简要总结

Our general objective, during this study, is to evaluate the feasibility and potential physiological benefits of using REBOA (resuscitative endovascular balloon occlusion of the aorta) CPR (cardiopulmonary resuscitation) for patients presenting with a cardiac arrest to a community hospital. This would represent the first step for doing a larger, randomized clinical trial on the use of REBOA in non-traumatic cardiac arrest.

详细描述

Primary objective: Validate the feasibility of using REBOA in a community hospital setting during cardiac arrest as an adjunct to ACLS (advances cardiac life support) . This will be done by measuring time to REBOA placement and successful inflation. Furthermore, we will also document any REBOA related complications.

Secondary objectives: Evaluate the potential physiological benefits of REBOA for human subjects in NTCA (non traumatic cardiac arrest) that are not responding to standard ACLS.

Study Design and Methodology Trial design The trial is a single-center, single-arm, open (unblinded), feasibility, experimental study.

Study Duration The study is expected to begin in winter 2022 and last approximately 12 months. Population studied The population studied will be patients in non-traumatic cardiac arrest at Santa Cabrini Hospital, aged 18-75 years old.

Patients presenting with a witnessed cardiac arrest (out of hospital cardiac arrest (OHCA) or in hospital cardiac arrest (IHCA)) and in which ACLS was performed for at least 15 minutes or BLS for at least 30 minutes and for no more than 60 minutes will be evaluated for eligibility to participate in the study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • - Patients aged 18-75 years old
  • Suspected reversible cause of cardiac arrest (except for trauma), with one of any of the following prognostic signs30
  • Reactive pupils
  • Agonal breathing
  • EtCO2>10 mmHg
  • Any cardiac activity on bedside echocardiogram
  • Body habitus accommodating automated Lund University Cardiac Arrest System (LUCAS)
  • Level of care includes CPR, or unable to obtain level of care (if possible, validate with relative)
  • More than 15 minutes of ACLS with no ROSC or more than 30 minutes of BLS with no ROSC

排除标准

  • Transfer accepted for ECPR
  • History of severe dementia
  • Advance Medical Directives against resuscitation
  • History of aortic pathology or surgery
  • LUCAS not compatible with the patient's body habitus
  • Pregnancy
  • Any illness resulting in loss of independent living capacity
  • Severe cardiopulmonary disease
  • Aortic dissection, aortic aneurysm, tension pneumothorax or tamponade seen on TEE/TTE
  • Strangulation
  • Suspected intracerebral hemorrhage
  • Accidental hypothermia
  • More than 60 minutes of resuscitation

结局指标

主要结局

success rate and time of REBOA inflation during non-traumatic arrest in a community hospital

时间窗: 1 year

● Feasibility of intra-arrest REBOA catheter placement and zone 1 inflation in NTCA in a community hospital setting

次要结局

  • blood pressure(0-15 min per study over a year)
  • cerebral saturation(0-15 min per study over a year)
  • TEE-guided REBOA positioning(5 minutes per study over 1 year)
  • ETCO2(0-15 min per study over a year)
  • ROSC(0-30 min per study over a year)
  • 7 day survival(7 days over a year)

研究者

发起方
Ciusss de L'Est de l'Île de Montréal
申办方类型
Other
责任方
Sponsor

相似试验