跳至主要内容
临床试验/NCT00248443
NCT00248443已完成3 期

Severe Acute Respiratory Failure in Hematology and Cancer Patients Without Bronchoalveolar Lavage. A Multicentric Randomized Controlled Trial

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 206 人开始时间: 2005年8月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
206
试验地点
2
主要终点
Reduction in intubation rate

研究概览

简要总结

The MiniMax® study is a multicenter randomized controlled study aimed at demonstrating that a combination of non-invasive diagnostic tools are as effective as fiberoptic bronchoscopy and bronchoalveolar lavage (FO-BAL) in performing the etiological diagnosis of acute respiratory failure in cancer patients.

详细描述

Acute respiratory failure is a dreadful complication in cancer patients. Indeed, about 20% of the patients will present with pulmonary infiltrates, but Intensive Care Unit (ICU) admission and mechanical ventilation will be needed in half of them resulting in mortality for most of the patients. Managing cancer patients with respiratory failure implicates three mandatory tasks: 1) early antibiotics administration covering suspected pathogens; 2) search for the actual aetiology; and 3) adequate supportive care with access to invasive or non invasive respiratory support. Performing the etiological diagnosis is crucial. Fiberoptic bronchoscopy and bronchoalveolar lavage (FO-BAL) remains the cornerstone of the management of pulmonary infiltrates in cancer patients. However, non-invasive diagnostic tools have been validated in the recent years. Diagnostic and therapeutic impacts of FO-BAL are only of 30% to 60% and 15% to 60% respectively. In neutropenic patients and recipients of bone marrow or stem cell transplantation, this impact is significantly altered. Moreover, reports have highlighted significant rates of complications such as haemorrhage (5%), respiratory deterioration (11% to 40%), possibly heading to intubation and subsequent death. Therefore, balancing advantages to risks of FO-BAL is in order. The MiniMax® study is a multicenter randomized controlled study aimed at demonstrating that a combination of non-invasive diagnostic tools are as effective as FO-BAL in performing the etiological diagnosis of acute respiratory failure in cancer patients. In addition, these non-invasive tests might not lead to deterioration of the respiratory status and corresponding requirement to intubation and mechanical ventilation. The group of investigators is used to manage cancer patients with pulmonary involvement. In the 21 centres, patients will be randomized to be managed either with FO-BAL or with only non-invasive tools. In each case, patients will be managed with the best supportive care including adequate antibiotics, respiratory support and all needed life sustaining therapies. Our hypothesis is to reduce intubation rate using a non-invasive approach (without FO-LBA). Surrogate markers will be hospital mortality and the number of diagnostic procedures in each group of patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
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

  • Patients with a malignant haemopathy or a cancer
  • Patients with severe acute respiratory failure requiring admission to an ICU
  • No argument for a congestive cardiac insufficiency (heart failure)
  • Patients who provided their informed consent

排除标准

  • Age less than 18
  • Patient who refuses to undergo fiberoptic bronchoscopy
  • Therapeutic limitation
  • Patients intubated at ICU admission
  • Etiological diagnosis of the acute respiratory failure known
  • Lack of available bronchoscopy
  • Post-operative direct admission
  • Inclusion in another research protocol in the ICU (HURRIET law)

结局指标

主要结局

Reduction in intubation rate

时间窗: 28 days

次要结局

  • Mortality at 28 days(28 days)
  • Hospital mortality(28 days)
  • Duration of mechanical ventilation (invasive or non invasive)(28 days)
  • Psychological aftereffects(28 days)

研究者

申办方类型
Other

研究点 (2)

Loading locations...

相似试验

Réa-MiniMax: Severe Acute Respiratory Failure in... | 临床试验