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meta分析 对照试验 多中心研究 工程量 临床试验 临床治疗 流程图 民事诉讼 平行 清单 权威 双盲法 随机对照试验 条目 系统评价 细菌感染 刑事诉讼 循证医学 医疗卫生 证据

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首页 > 学术期刊 > 中华流行病学杂志 > 2006年12期 > 如何撰写高质量的流行病学研究论文第四讲随机平行对照试验报告规范——CONSORT介绍

如何撰写高质量的流行病学研究论文第四讲随机平行对照试验报告规范——CONSORT介绍

随机对照试验为临床治疗和医疗卫生干预提供重要证据.对随机对照试验的严格评价有赖于充分、准确的报告.临床试验报告统一标准(CONSORT)清单和流程图是当前公认的、最权威的随机平行对照试验的报告规范.本文介绍该清单和流程图的内容,并对一些重要条目进行了详细说明.

作 者：
王波 詹思延  
作者单位：
100083,北京大学医学部公共卫生学院流行病学与卫生统计学系 
刊 名：
中华流行病学杂志  ISTIC PKU
英文刊名：
CHINESE JOURNAL OF EPIDEMIOLOGY 
年，卷(期)：
2006 27(12) 
分类号：
H1 
关键词：
临床试验报告统一标准 知识脉络  随机对照试验 知识脉络  清单 知识脉络  流程图 知识脉络 
机标分类号：
R57 R76 
机标关键词：
质量流行病学研究论文平行对照试验随机对照试验流程图临床试验报告医疗卫生严格评价清单临床治疗报告规范证据预提条目权威标准 
基金项目：
 
DOI：
 
参考文献(19条)
  1. Begg C.Cho D.Eastwood S Improving the quality of reporting of randomized controlled trials.The CONSORT statement 1996
  2. Moher D.Schulz KF.Altman DG The CONSORT statement:revised recommendations for improving the quality of reports of parallel group randomized trials 2001
  3. DerSimonian R.Charette LJ.McPeek B Reporting on methods in clinical trials 1982
  4. Pocock SJ.Hughes MD.Lee RJ Statistical problems in the reporting of clinical trials.A survey of three medical journals 1987
  5. Moher D.Dulberg CS.Wells GA Statistical power,sample size,and their reporting in randomized controlled trials 1994
  6. Hollis S.Campbell F What is meant by intention to treat analysis? Survey of published randomised controlled trials 1999
  7. Schulz KF.Chalmers I.Grimes DA Assessing the quality of randomization from reports of controlled trials published in obstetrics and gynecology journals 1994
  8. Hotopf M.Lewis G.Normand C Putting trials on trial-the costs and consequences of small trials in depression:a systematic review of methodology 1997
  9. Altman DG.Schulz KF.Moher D The revised CONSORT statement for reporting randomized trials:explanation and elaboration 2001
  10. Schulz KF.Chalmers I.Hayes RJ Empirical evidence of bias.Dimensions of methodological quality associated with estimates of treatment effects in controlled trials 1995
  11. Schulz KF Subverting randomization in controlled trials 1995
  12. Gφtzsche PC Blinding during data analysis and writing of manuscripts 1996
  13. The standards of reporting trials group A proposal for structured reporting of randomized controlled trials 1994
  14. Schulz KF.Grimes DA.Altman DG Blinding and exclusions after allocation in randomised controlled trials:survey of published parallel group trials in obstetrics and gynaecology 1996
  15. Matthews JN.Altman DG Statistics notes.interaction 2:compare effect sizes not P values 1996
  16. Assmann SF.Pocock SJ.Enos LE Subgroup analysis and other (mis) uses of baseline data in clinical trials 2000
  17. Wallen L.Swahn E.Kontny F For FRISC Ⅱ investigators.Invasive compared with non-invasive treatment in unstable coronaryartery disease:FRISC Ⅱ prospective randomised multicentre study 1999
  18. Lachin JL Statistical considerations in the intent-to-treat principle 2000
  19. Moher D.Jones A.Lepage L Use of the CONSORT statement and quality of reports of randomized trials:a comparative before and after evaluation? 2001

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