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临床试验/NCT00290602
NCT00290602已完成2 期

Prospective Phase II Study of Early Low Dose Steroid Therapy of Acute Respiratory Distress Syndrome (ARDS) After Thoracic Surgery (E-START)

National Cancer Center, Korea2 个研究点 分布在 2 个国家目标入组 40 人开始时间: 2004年2月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
40
试验地点
2
主要终点
the percentage of patients alive at postoperative 30 day; Patients discharged alive from the hospital in unassisted breathing before 60 days

研究概览

简要总结

The purpose of this study is to determine whether the 2mg/kg administration of corticosteroids, in the form of methylprednisolone sodium succinate, in early phase acute respiratory distress syndrome after thoracic surgery, will reduce the postoperative mortality.

详细描述

The acute respiratory distress syndrome (ARDS) developing after thoracic surgery is usually a lethal complication. The use of corticosteroid in ARDS has been the subject of great controversy and debate over the years. Unfortunately, trials of short-term, high-dose steroid therapy failed to show an improvement in mortality of patients at risk of, or with early, ARDS. Several investigators have suggested that the use of corticosteroids in the late or fibroproliferative phase of ARDS improved lung function and survival.

Recently some authors have demonstrated that there is a potential for pulmonary fibroproliferation during the early stages of ARDS and the use of low-dose corticosteroids at these early stages has been found to lead to a complete maintenance of in vivo and in vitro respiratory mechanics in acute lung injury. These articles had important implications both for the study of repair mechanisms and the timing of therapies.

研究设计

研究类型
Interventional
分配方式
Non Randomized
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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ARDS, defined as the acute onset of:
  • PaO2/FiO2 ≤
  • Bilateral infiltrates. The infiltrates may be patchy, diffuse, homogeneous, or asymmetric, and should be consistent with pulmonary edema or the fibrotic changes of fibroproliferation. Opacities due to pleural effusions or atelectasis should not be considered. If pneumonectomy, unilateral infiltrate is included.
  • No evidence of left atrial hypertension. If measured, PAWP ≤ 18 mmHg.
  • Criteria a-c must occur together within a 24-hour interval. The first date that these criteria are met is defined as the onset of ARDS
  • Since ARDS onset, chest infiltrates must be progressive, and chest computed tomographic scan findings are consistent with postoperative ARDS findings or ground glass opacities by radiologists.
  • Major thoracic surgery
  • Lung cancer; pneumonectomy, extended pneumonectomy, lobectomy, sleeve lobectomy, extended lobectomy, wedge resection.
  • Esophageal cancer; Ivor-Lewis operation, transhiatal esophagectomy, McKeown operation.
  • Metastatic lung cancer; simultaneous bilateral metastasectomy.
  • PaO2/FiO2 ≤ 200 on the day of E-START enrollment.

排除标准

  • Clinical evidence of active and untreated infection.
  • Clarifications:
  • A known, undrained abscess (e.g. Staphylococcal lung abscess or loculated empyema or intra-abdominal abscess) or a known intravascular nidus of infection (e.g., bacterial or fungal endocarditis) will be a basis for exclusion, even if it is being treated with antibiotics.
  • A bacterial infection being treated with a standard antibiotic regimen would not be a basis for exclusion.
  • Disseminated fungal infection, even if being treated, is an exclusion.
  • Ongoing septic shock, even if on antibiotics is a basis for exclusion.
  • Age <18 years.
  • Burns requiring skin grafting.
  • Patients with AIDS by CDC criteria, diagnosed by either a documented AIDS defining illness or CD4<200(see Appendix F); prednisolone therapy >=300mg(or its equivalent) cumulative dose within 21 days prior to enrollment, or >15mg/day(or its equivalent) within 7 days prior to enrollment; cytotoxic therapy within 3 weeks.
  • Other irreversible chronic disease or condition for which 6 month mortality is estimated ≥ 50%.
  • Not committed to full support.
  • Severe chronic liver disease (Child-Pugh Class C score>10 points).
  • Transplant patients with the exception of autologous bone marrow transplants.
  • Extracorporeal support of gas exchange at the time of study entry (e.g., ECMO).
  • Known or suspected adrenal insufficiency.
  • Vasculitis with diffuse alveolar hemorrhage.

结局指标

主要结局

the percentage of patients alive at postoperative 30 day; Patients discharged alive from the hospital in unassisted breathing before 60 days

次要结局

  • the percentage of ventilator-free patients at 7 days from study entry; the percentage of oxygen-independent patients at 21 days following study entry; response of inflammatory mediators to the novel treatment; pulmonary function in ARDS survivors

研究者

申办方类型
Other Gov

研究点 (2)

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