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Impact of an Early Palliative Approach (LATAREA-IV)

2017年6月19日 更新者:Assistance Publique - Hôpitaux de Paris

Impact of a Computer-assisted Tool to Help Reflection on the Decision to Withhold or to Withdraw Treatments for Surgical Patients in Intensive Care Units

Rationale: Medicalized end of life rose profound society questions and debates. Major Laws and scientific society recommendations emerged from those reflections. These texts help withholding/withdrawing life-sustaining treatments allowing a palliative approach and to favor comfort treatments for end of life patients.

Main Objective: To evaluate the impact of a procedure to support reflection on the level of therapeutic involvement for surgical patient (who undergone surgery or not) in ICU after having identified vulnerability criteria early.

Secondary objectives: To assess the usual care of the control group and the impact of the procedure according to ICU type (medical, surgical, mixed); the characteristics of surgical patients concerned by a palliative strategy; the impact of an incentive approach on length of mechanical ventilation and length of stay in the ICU; To measure the extent of information collected concerning the collegial process; the impact of the procedure on caregivers' satisfaction; To count the number of identified conflicts Study type: Prospective, controlled, cluster randomized study of routine care Purpose: Study the implementation of the Act "Leonetti" released on 22 April 2005 calling for a compassionate approach and palliative care for patients at end of life.

Inclusion criteria: Surgical patients (who undergone surgery or not) hospitalized in ICU during the study period Non-inclusion criteria: Patients hospitalized less than 24h; non-surgical patients; patients who don't need ICU care or surveillance; minors; brain-dead patients (at the time of admission) Primary endpoint: Rate of deaths with palliative strategy (withholding or withdrawing treatments) Randomization process: each center is randomized adjusting on type of ICU (medical, surgical, mixed) and number of annual hospitalization volume.

  • Control group: ICU usual care
  • Intervention group: vulnerability criteria lead to reflection on level of therapeutic involvement, with the help of a written guide.

Number of patients: 2750 surgical patients Number of centers: 45 Study design: usual data will be collected in a secured web-based Case Report Form (CRF) at ICU admission and each time therapeutic strategy will change. Additional data will be collected for the intervention group according to the initial presence or the later apparition of predefined criteria, a standardized reflection procedure will start helped by the implementation of a guide for collegial approach and decision making.

Length: 30 months

研究概览

研究类型

介入性

注册 (实际的)

1172

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Suresnes、法国、92 150
        • Hopital Foch

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Surgical patients (who undergone surgery or not) hospitalized in ICU during the study period
  • No opposition to the use of data collected from the patient or a relative or inclusion in emergency and non-opposition collected offline

Exclusion Criteria:

  • Patients admitted legally dead or brain-dead

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
无干预:Group A
the centres applies their usual practices
其他:Group B
strategy promoting early consideration and collegiate vulnerability of patients
One day training with the provision of vulnerability criteria inciting an early reflection of the level of therapeutic engagement; sheets available on the internet computer support collegial reflection and traceability of decisions to limit and stop treatments, incorporating the provisions of law known Leonetti

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Number of participants dead with palliative strategy
大体时间:From ICU hospitalization to 6 months after inclusion
Rate of death with collegial process and withdrawing/withholding treatment
From ICU hospitalization to 6 months after inclusion

次要结果测量

结果测量
大体时间
Impact of the procedure according to ICU type
大体时间:From ICU hospitalization to 6 months after inclusion
From ICU hospitalization to 6 months after inclusion
Characteristics of surgical patients concerned by a palliative strategy
大体时间:From ICU hospitalization to 6 months after inclusion
From ICU hospitalization to 6 months after inclusion
Impact of an incentive approach on length of mechanical ventilation and length of stay in the ICU.
大体时间:From ICU hospitalization to 6 months after inclusion
From ICU hospitalization to 6 months after inclusion
Extent of information collected concerning the collegial process
大体时间:From ICU hospitalization to 6 months after inclusion
From ICU hospitalization to 6 months after inclusion
Impact of the procedure on caregivers' satisfaction
大体时间:From ICU hospitalization to 6 months after inclusion
From ICU hospitalization to 6 months after inclusion
Number of identified conflicts
大体时间:From ICU hospitalization to 6 months after inclusion
From ICU hospitalization to 6 months after inclusion

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Edouard FERRAND, MD、Hopital Foch

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2012年10月1日

初级完成 (实际的)

2014年1月1日

研究完成 (实际的)

2015年12月1日

研究注册日期

首次提交

2015年6月1日

首先提交符合 QC 标准的

2015年6月10日

首次发布 (估计)

2015年6月15日

研究记录更新

最后更新发布 (实际的)

2017年6月20日

上次提交的符合 QC 标准的更新

2017年6月19日

最后验证

2017年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • K071203

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

Criteria of Vulnerability的临床试验

3
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