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临床试验/NCT02471976
NCT02471976已完成不适用

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

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 1,172 人开始时间: 2012年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,172
试验地点
2
主要终点
Number of participants dead with palliative strategy

研究概览

简要总结

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

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

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

入选标准

  • 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

排除标准

  • Patients admitted legally dead or brain-dead

结局指标

主要结局

Number of participants dead with palliative strategy

时间窗: From ICU hospitalization to 6 months after inclusion

Rate of death with collegial process and withdrawing/withholding treatment

次要结局

  • Impact of the procedure according to ICU type(From ICU hospitalization to 6 months after inclusion)
  • Characteristics of surgical patients concerned by a palliative strategy(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.(From ICU hospitalization to 6 months after inclusion)
  • Extent of information collected concerning the collegial process(From ICU hospitalization to 6 months after inclusion)
  • Impact of the procedure on caregivers' satisfaction(From ICU hospitalization to 6 months after inclusion)
  • Number of identified conflicts(From ICU hospitalization to 6 months after inclusion)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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