To Improve the Quality of Clinical Trials by Promote Clinical Trial Registration and Good Publication Practice_Chinese Journal of Evidence-Based Medicine

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李幼平 , 杜亮 , 刘雪梅

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DOI：

10.7507/1672-2531.20100004

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Citation： 李幼平,杜亮,刘雪梅. To Improve the Quality of Clinical Trials by Promote Clinical Trial Registration and Good Publication Practice. Chinese Journal of Evidence-Based Medicine, 2010, 10(1): 1-2. doi: 10.7507/1672-2531.20100004 Copy

1.	Moher D, Schulz KF, Altman DG. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomized trials. Lancet, 2001, 357: 1191-1194.
2.	Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med, 2009, 151(4): 264-269.
3.	Fernández E. Observational studies in Epidemiology (STROBE). Med Clin (Barc), 2005, 125(Supl.1): 43-48.
4.	Ad Hoc Working Group. A proposal for more informative abstracts of clinical articles. Annual of Internation Medicine, 1987, 106: 598-604.
5.	Standards of Reporting Trials Group. A proposal for structured reporting of randomized controlled trials. JAMA, 1994, 272(24): 1926-1931.
6.	Working group on recommendations for reporting of clinical trials in the biomedical literature. Call for comments on a proposal to improve reporting of clinical trials in the biomedical literature: a position paper. Ann Intern Med, 1994, 121(11): 894-895.
7.	Begg C, Cho M, Eastwood S, et al. Improving the quality of reporting of randomized controlled trials. JAMA, 1996, 276(8): 637-639.
8.	Extensions of the CONSORT Statement. [2010-01-03]. http://www. consort-statement.org/extensions/.
9.	杜亮, 陈耀龙, 陈敏, 等. 从CONSORT到GPP: 医学研究报告规范简介. 编辑学报, 2008(4): 367-370.
10.	Laine C, Horton R, DeAngelis C, et al. International Committee of Medical Journal Editors (ICMJE). Clinical trial registration: looking back and moving ahead. Lancet, 2007, 369(9577): 1909-1911.
11.	Ghersi D, Pang T. 从墨西哥到马里: 临床试验注册发展历程四年回顾. 中国循证医学杂志, 2009, 9(2): 123-126.

1. Moher D, Schulz KF, Altman DG. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomized trials. Lancet, 2001, 357: 1191-1194.
2. Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med, 2009, 151(4): 264-269.
3. Fernández E. Observational studies in Epidemiology (STROBE). Med Clin (Barc), 2005, 125(Supl.1): 43-48.
4. Ad Hoc Working Group. A proposal for more informative abstracts of clinical articles. Annual of Internation Medicine, 1987, 106: 598-604.
5. Standards of Reporting Trials Group. A proposal for structured reporting of randomized controlled trials. JAMA, 1994, 272(24): 1926-1931.
6. Working group on recommendations for reporting of clinical trials in the biomedical literature. Call for comments on a proposal to improve reporting of clinical trials in the biomedical literature: a position paper. Ann Intern Med, 1994, 121(11): 894-895.
7. Begg C, Cho M, Eastwood S, et al. Improving the quality of reporting of randomized controlled trials. JAMA, 1996, 276(8): 637-639.
8. Extensions of the CONSORT Statement. [2010-01-03]. http://www. consort-statement.org/extensions/.
9. 杜亮, 陈耀龙, 陈敏, 等. 从CONSORT到GPP: 医学研究报告规范简介. 编辑学报, 2008(4): 367-370.
10. Laine C, Horton R, DeAngelis C, et al. International Committee of Medical Journal Editors (ICMJE). Clinical trial registration: looking back and moving ahead. Lancet, 2007, 369(9577): 1909-1911.
11. Ghersi D, Pang T. 从墨西哥到马里: 临床试验注册发展历程四年回顾. 中国循证医学杂志, 2009, 9(2): 123-126.

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