CONSORT Revised - Improving the reporting of randomized trials

JAMA

Volumn 285, Issue 15, 2001, Pages 2006-2007

  Rennie, D ^a  

^a JAMA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL RESEARCH; CLINICAL TRIAL; EDITORIAL; HUMAN; MEDICAL LITERATURE; PRACTICE GUIDELINE; PRIORITY JOURNAL; PUBLICATION; QUALITY CONTROL; RANDOMIZATION; STANDARD;

EID: 0035906289     PISSN: 00987484     EISSN: None     Source Type: Journal    
DOI: 10.1001/jama.285.15.2006     Document Type: Editorial

References (21)

1. Empirical evidence of bias
2. A proposal for structured reporting of randomized controlled trials
3. Call for comments on a proposal to improve reporting of clinical trials in the biomedical literature
4. Randomized controlled trial of 3 versus 10 days of trimethoprim/sulfamethoxazole for acute maxillary sinusitis
5. Reporting randomized controlled trials: An experiment and a call for responses from readers
6. Improving the quality of reporting of randomized controlled trials: The CONSORT statement
7. How to report randomized controlled trials: The CONSORT statement
8. CONSORT statement on the reporting standards in clinical trials
9. CONSORT statement on the reporting standards of clinical trials
10. Improving the quality of reports of meta-analyses of randomised controlled trials: The QUOROM statement
11. Meta-analysis of observational studies in epidemiology: A proposal for reporting
12. Use of the CONSORT statement and quality of reports of randomized trials: A comparative before-and-after evaluation
13. Beyond CONSORT
14. CONSORT: An evolving tool to help improve the quality of reports of randomized controlled trials
15. Value of flow diagrams in reports of randomized controlled trials
16. The CONSORT statement: Revised recommendations for improving the quality of reports of parallel-group randomized trials
17. The revised CONSORT statement for reporting randomized trials: Explanation and elaboration
18. CONSORT statement on the reporting standards of clinical trials: MRC uses checklist similar to CONSORT's
19. Physician interpretations and textbook definitions of blinding terminology in randomized controlled trials
20. Fair conduct and fair reporting of clinical trials