Abstract
Timely dissemination of results from clinical studies is crucial for the advancement of knowledge and clinical decision making. A large body of research has shown that up to half of clinical trials do not publish their findings. In this study, we sought to determine whether clinical trial publication rates within neurology have increased over time. Focusing on neurology clinical trials completed between 2008 to 2014, we found that while the overall percentage of published trials has not changed (remaining at approximately 50%), time to publication has significantly decreased. Our findings suggest that clinical trials within neurology are being published in a more timely manner.
Introduction
Clinical trials are an integral part of translating scientific findings and improve patient outcomes. Thus, dissemination of clinical trials results is crucial for informing public health policy and clinical decision making. However, dissemination rates of clinical trials results are disappointing: 25-50% of clinical trial results are not published [1, 2]. Within the field of neurology, we previously found that approximately only half of clinical trials published their findings in peer-reviewed journals [3]. In recognition of this major public health dilemma, governmental policies have been implemented to improve dissemination of clinical research results, including the 2007 US FDA Amendment Act (FDAAA) mandating clinical trial registration and results reporting on ClinicalTrials.gov a publicly accessible clinical registry, for all trials of FDA-regulated products [4, 5]. In this study, we sought to expand upon our previous findings to characterize trends in publication of clinical trials within the field of neurology. Specifically, we sought to determine: 1) Trends in the percentage of completed trials that published their findings from 2008 to 2014, and 2) Trends in the overall time to publication following trial completion.
Methods
Data analysis was conducted using a database that we generated [3]. Briefly, we performed a search on July 19, 2016, through ClinicalTrials. gov for interventional trials conducted within the United States between 2007 and 2014 using the search term “nervous system disease.” Publication status was verified using the associated ClinicalTrials.gov webpage and the SCOPUS (Elsevier) database. We first grouped neurology clinical trials into the years when they were completed (2008 to 2014). For each year, we calculated the percentage of completed clinical trials that published their findings and the time to publication (defined as months between publication date and the primary completion date). To analyze trends in percent of completed trials that published their findings and time to publication, we used the Chi-Square test for trend and the Ordinary one-way ANOVA test followed by Tukey’s multiple comparisons test, respectively. All statistical tests were conducted using GraphPad Prism.
Results
Table 1 shows the number of completed and published trials per year from 2008 to 2014. Overall, we did not find any trends in percentage of published clinical trials from 2008 to 2014, as the publication rates per year remained at approximately 50% (p = 0.2615) (Figure 1A) For published trials, we found that the overall time to publication decreased from 2008 -2014 (p < 0.0001) (Figure 1B) For example, time to publication for published trials completed in 2008 was 34.59 ± 2.30 months, whereas time to publication for published trials completed in 2014 was only 18.79 ± 0.95 months (p < 0.0001) (Figure 1B)

Clinical trial publication trends within neurology. A) Trends in percentage of published neurology clinical trials from 2008 to 2014. Chi-square test for trend was used to determine the p value. B) Trends in time to publication (in months between publication date and primary completion date) of neurology clinical trials from 2008 to 2014. One-way ANOVA test was used to determine the p value. Mean ± SEM are shown for each year.
Number of completed and published trials per year from 2008 to 2014.
Year | Number of completed trials within year | Number of published trials within year |
---|---|---|
2008 | 172 | 82 |
2009 | 242 | 100 |
2010 | 284 | 157 |
2011 | 358 | 182 |
2012 | 406 | 207 |
2013 | 394 | 171 |
2014 | 193 | 81 |
Discussion
Clinical trials are crucial for the translation of scientific discoveries into diverse areas of clinical medicine. Thus, timely dissemination of clinical trial results is important for the scientific progress by informing future research and medical practice. We found that while the overall percentage of clinical trials that published their findings has not changed, the time to publication has significantly decreased from 2008 to 2014. These findings suggest that despite no overall improvements in publication rates, clinical trials in neurology are being published in a more timely manner following study completion.
Although the scientific and medical communities have now recognized low publication of clinical trials to be a major problem [2, 6], the reasons underlying the failure to report clinical trial results are not understood. In a study that extensively reviewed controlled clinicals in fragile X syndrome [7], the most translated neurodevelopmental disorder [8], some large well-powered clinical trial studies remain unpublished, while others took some time to be published as they showed “failed” primary outcomes. The difficulty in publishing trials with inconclusive and negative results may thus explain why approximately half of neurology clinical trials are not published [3]. Indeed, clinical trials with positive findings were more likely to be recommended for publication compared to those with negative findings [9]. However, regardless of outcomes, timely reporting of all research findings is an important duty to the public and to patients that researchers need to uphold so that clinical science can progress [6]. Future investigations should seek to determine the underlying mechanisms that explain low rates of publication in clinical trials and thus help to define better research practice policies to ensure timely dissemination of clinical trial results.
Acknowledgements
PQD was supported by NIH Medical Scientist Training Program Training Grant T32GM007205. KNS was supported by the NIH, AHA, Bard, Biogen, Novartis, Astrocyte, and Hyperfine.
References
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[2] Chen, R., et al., Publication and reporting of clinical trial results: cross sectional analysis across academic medical centers BMJ, 2016. 352: p. i637.10.1136/bmj.i637Search in Google Scholar PubMed PubMed Central
[3] Sreekrishnan, A., et al., Publication and Dissemination of Results in Clinical Trials of Neurology JAMA Neurol, 2018. 75(7): p. 890-891.10.1001/jamaneurol.2018.0674Search in Google Scholar PubMed PubMed Central
[4] Phillips, A.T., et al., Association of the FDA Amendment Act with trial registration, publication, and outcome reporting Trials, 2017. 18(1): p. 333.10.1186/s13063-017-2068-3Search in Google Scholar PubMed PubMed Central
[5] The Food and Drug Administration Amendments Act (FDAAA) in Public Law: 110-85 T.F.a.D. Administration, Editor. 2007.Search in Google Scholar
[6] Wallach, J.D. and H.M. Krumholz, Not Reporting Results of a Clinical Trial Is Academic Misconduct Ann Intern Med, 2019.10.7326/M19-1273Search in Google Scholar PubMed
[7] Budimirovic, D.B., et al., Updated report on tools to measure outcomes of clinical trials in fragile X syndrome J Neurodev Disord, 2017. 9: p. 14.10.1186/s11689-017-9193-xSearch in Google Scholar PubMed PubMed Central
[8] Duy, P.Q. and D.B. Budimirovic, Fragile X Syndrome: Lessons Learned from the Most Translated Neurodevelopmental Disorder in Clinical Trials Transl Neurosci, 2017. 8: p. 7-8.10.1515/tnsci-2017-0002Search in Google Scholar PubMed PubMed Central
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© 2019 Phan Q. Duy et al. published by De Gruyter
This work is licensed under the Creative Commons Attribution 4.0 International License.
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Articles in the same Issue
- Autobiographical memory increases pupil dilation
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- Nox2-dependent neuroinflammation in an EAE model of multiple sclerosis
- Radiation outcome in mechanical thrombectomy of acute ischemic stroke
- Test and evaluation of advertising effect based on EEG and eye tracker
- Difference in the ascending reticular activating system injury between mild traumatic brain injury and cerebral concussion
- Early antiinflammatory therapy attenuates brain damage after sah in rats
- Change of cognitive functions after stroke with rehabilitation systems
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- MiR-1906 attenuates neuropathic pain in rats by regulating the TLR4/mTOR/ Akt signaling pathway
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- Early multidisciplinary intensive-care therapy can improve outcome of severe anti-NMDA-receptor encephalitis presenting with extreme delta brush
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