The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
SPIRIT 2013: new guidance for content of clinical trial protocols
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In the citing paper
“The investigation will be conducted at La Paz University Hospital (Madrid, Spain) in accordance with SPIRIT 2013 [25, 26] and CONSORT 2010 [27] statements.”
Citations
Cites
SPIRIT 2013 Statement: Defining Standard Protocol Items for Clinical Trials
Chan, A.-W., Tetzlaff, J. M., Altman, D. G., Laupacis, A., Gøtzsche, P. C., Krleža-Jerić, K., Hróbjartsson, A., Mann, H., Dickersin, K., Berlin, J. A., et al. (2013) · Annals of Internal Medicine · doi:10.7326/0003-4819-158-3-201302050-00583 · Cited by 7,363
Self-citationSPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials
Chan, A.-W., Tetzlaff, J. M., Gotzsche, P. C., Altman, D. G., Mann, H., Berlin, J. A., Dickersin, K., Hrobjartsson, A., Schulz, K. F., Parulekar, W. R., et al. (2013) · BMJ · doi:10.1136/bmj.e7586 · Cited by 6,251
Self-citationThe prevention and treatment of missing data in clinical trials
Little, R. J., D'Agostino, R., Cohen, M. L., Dickersin, K., Emerson, S. S., Farrar, J. T., Frangakis, C., Hogan, J. W., Molenberghs, G., Murphy, S. A., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmsr1203730 · Cited by 1,884
Self-citationChan, A.-W., Hróbjartsson, A., Haahr, M. T., Gøtzsche, P. C., & Altman, D. G. (2004) · JAMA · doi:10.1001/jama.291.20.2457 · Cited by 1,845
Self-citationTurner, L., Shamseer, L., Altman, D. G., Schulz, K. F., & Moher, D. (2012) · Systematic Reviews · doi:10.1186/2046-4053-1-60 · Cited by 628
Self-citationComparison of protocols and registry entries to published reports for randomised controlled trials
Dwan, K., Altman, D. G., Cresswell, L., Blundell, M., Gamble, C. L., & Williamson, P. R. (2011) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.mr000031.pub2 · Cited by 243
Self-citationFrequency and reasons for outcome reporting bias in clinical trials: interviews with trialists
Smyth, R. M. D., Kirkham, J. J., Jacoby, A., Altman, D. G., Gamble, C., & Williamson, P. R. (2011) · BMJ · doi:10.1136/bmj.c7153 · Cited by 220
Self-citationAdverse Event Reporting in Publications Compared With Sponsor Database for Cancer Clinical Trials
Scharf, O., & Colevas, A. D. (2006) · Journal of Clinical Oncology · doi:10.1200/jco.2005.05.3959 · Cited by 111
Guidelines for randomized clinical trial protocol content: a systematic review
Tetzlaff, J., Chan, A., Kitchen, J., Sampson, M., Tricco, A. C., & Moher, D. (2012) · Systematic Reviews · doi:10.1186/2046-4053-1-43 · Cited by 89
Self-citationMeasuring the Incidence, Causes, and Repercussions of Protocol Amendments
Getz, K. A., Zuckerman, R., Cropp, A. B., Hindle, A. L., Krauss, R., & Kaitin, K. I. (2011) · Drug Information Journal · doi:10.1177/009286151104500307 · Cited by 76
Developing a guideline for clinical trial protocol content: Delphi consensus survey
Tetzlaff, J., Moher, D., & Chan, A. (2012) · Trials · doi:10.1186/1745-6215-13-176 · Cited by 74
Self-citationComparison of protocols and registry entries to published reports for randomised controlled trials
Dwan, K. M., Altman, D. G., Blundell, M., Gamble, C. L., & Williamson, P. R. (2010) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.mr000031 · Cited by 59
Self-citationBollyky, T. J., Cockburn, I., & Berndt, E. R. (2010) · Clinical Trials · doi:10.1177/1740774510386390 · Cited by 35
Access to data in industry-sponsored trials
Lundh, A., Krogsbøll, L. T., & Gøtzsche, P. C. (2011) · The Lancet · doi:10.1016/s0140-6736(11)61871-0 · Cited by 28
Decullier, É., Lhéritier, V., & Chapuis, F. R. (2005) · BMC Medical Ethics · doi:10.1186/1472-6939-6-9 · Cited by 24
Russ, H., Busta, S., Riedel, A., Zöllner, G., & Jost, B. (2009) · PubMed Central · doi:10.3205/000066 · Cited by 13
Research works printed but not linked: 1
- Russ, 2009, Ger Med Sci, 7, Doc07
Cited by
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Increasing value and reducing waste: addressing inaccessible research
Chan, A.-W., Song, F., Vickers, A., Jefferson, T., Dickersin, K., Gøtzsche, P. C., Krumholz, H. M., Ghersi, D., & van der Worp, H. B. (2014) · The Lancet · doi:10.1016/s0140-6736(13)62296-5 · Cited by 887
Self-citationBlockchain technology for improving clinical research quality
Benchoufi, M., & Ravaud, P. (2017) · Trials · doi:10.1186/s13063-017-2035-z · Cited by 310
Strategies to improve retention in randomised trials
Brueton, V. C., Tierney, J., Stenning, S., Harding, S., Meredith, S., Nazareth, I., & Rait, G. (2013) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.mr000032.pub2 · Cited by 279
Lo, B. (2015) · JAMA · doi:10.1001/jama.2015.292 · Cited by 235
Chen, Y., Gao, Q., Zou, T., Wang, B., Liu, S., Sheng, J., Ren, J., Zou, X., Liu, Z., Song, Y., et al. (2020) · The Lancet. Gastroenterology & hepatology · doi:10.1016/s2468-1253(19)30409-1 · Cited by 210
Metadata
- Authors
- Chan, A.-W., Tetzlaff, J. M., Altman, D. G., Dickersin, K., & Moher, D.
- Affiliations
- University of Toronto (CA)
- Ottawa Hospital Research Institute (CA)
- University of Oxford (GB)
- Johns Hopkins University (US)
- University of Ottawa (CA)
- Corresponding author
- Chan, An-Wen
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 2013-01
- Volume
- 381
- Issue
- 9861
- Pages
- 91-92
- ISSN
- 0099-5355 (ISSN-L)
- 0140-6736
- OpenAlex
- W2031331450
- Cited by
- 298
- References
- 16
- Citations by year
- 2026: 11 · 2025: 21 · 2024: 40 · 2023: 34 · 2022: 23 · 2021: 27 · 2020: 24 · 2019: 37 · 2018: 22 · 2017: 19 · 2016: 15 · 2015: 10 · 2014: 9 · 2013: 6
- FWCI
- 13.54
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- The Lancet (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Social Sciences › Decision Sciences › Statistics, Probability and Uncertainty › Meta-analysis and systematic reviews
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Clinical practice guidelines implementation
- Keywords
- protocol modification, research ethics committees, clinical trial registration
- MeSH terms
- Clinical Trials as Topic, Humans, Practice Guidelines as Topic
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