跳至主要内容
临床试验/ISRCTN44351742
ISRCTN44351742已完成未知

Mesothelioma and Radical Surgery 2: a multicentre randomised trial comparing (extended) pleurectomy decortication versus no (extended) pleurectomy decortication for patients with malignant pleural mesothelioma.

Royal Brompton and Harefield NHS Foundation Trust0 个研究点目标入组 335 人开始时间: 2018年9月5日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
335

研究概览

简要总结

2020 Protocol article in https://pubmed.ncbi.nlm.nih.gov/32873681/ protocol (added 04/09/2020) 2024 Other publications in https://doi.org/10.1136/bmjopen-2023-079108 results from a complex recruitment intervention within the Mesothelioma and Radical Surgery 2 (MARS 2) study (added 20/05/2024)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Patient may enter study if ALL of the following apply:
  • 1. Aged 16 years or older
  • 2. Tissue (cytology or histology) confirmed epithelioid, sarcomatoid or biphasic mesothelioma*
  • 3. Disease confined to one hemi-thorax based on CT assessment
  • 4. Disease deemed surgically resectable**
  • 5. Fit for surgery**
  • 6. Capacity to provide written informed consent to participate in the trial
  • *The diagnosis” of mesothelioma is based on cytology and / or histopathology results as reviewed by MDT to be of sufficient certainty to recommend chemotherapy as treatment.
  • **To be confirmed by a surgeon at a MARS 2 surgical site (added 29/08/2019)

排除标准

  • Current inclusion criteria as of 29/08/2019:
  • Patient may not enter study if ANY of the following apply:
  • 1. Severe shortness of breath (this is defined as an Eastern Cooperative Oncology Group (ECOG) status >= 2, or if lung function tests are performed: pre-operative forced expiratory volume after one second (FEV1) or transfer factor of the lung for carbon monoxide (TLco) less than 20%);
  • 2. Serious concomitant disorder that would compromise participant safety during surgery (e.g. evidence of end organ failure)
  • 3. Severe heart failure (this is defined as NYHA III or IV or if an echocardiogram is performed an ejection fraction less than 30%)
  • 4. End stage kidney failure requiring dialysis
  • 5. Liver failure (e.g. encephalopathy and/or coagulation abnormalities)
  • 6. Prisoner
  • 7. Patient lacks capacity to consent
  • 8. Existing co-enrolment in another interventional clinical trial that aims to improve survival
  • Previous exclusion criteria:
  • Patient may not enter study if ANY of the following apply:
  • 1. Severe shortness of breath (Eastern Cooperative Oncology Group (ECOG) status >= 2, pre-operative forced expiratory volume after one second (FEV1) or transfer factor of the lung for carbon monoxide (TLco) less than 20%);
  • 2. Serious concomitant disorder that would compromise participant safety during surgery (e.g. evidence of end organ failure)
  • 3. Severe heart failure (EF less than 30% by echocardiogram)
  • 4. End stage kidney failure requiring dialysis
  • 5. Liver failure (e.g. encephalopathy and/or coagulation abnormalities)
  • 6. Prisoner
  • 7. Patient lacks capacity to consent
  • 8. Co-enrolment in another interventional clinical trial

研究者

相似试验