Adequate statistical power in clinical trials is associated with the combination of a male first author and a female last author

Publication date

2018-06-05

Authors

Otte, Willem M.ORCID 0000-0003-1511-6834ISNI 0000000389423861
Tijdink, Joeri K
Weerheim, Paul L
Lamberink, Herm
Vinkers, Christiaan H.ISNI 0000000390294462

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Abstract

Clinical trials have a vital role in ensuring the safety and efficacy of new treatments and interventions in medicine. A key characteristic of a clinical trial is its statistical power. Here we investigate whether the statistical power of a trial is related to the gender of first and last authors on the paper reporting the results of the trial. Based on an analysis of 31,873 clinical trials published between 1974 and 2017, we find that adequate statistical power was most often present in clinical trials with a male first author and a female last author (20.6%, 95% confidence interval 19.4-21.8%), and that this figure was significantly higher than the percentage for other gender combinations (12.5-13.5%; P<0.0001). The absolute number of female authors in clinical trials gradually increased over time, with the percentage of female last authors rising from 20.7% (1975-85) to 28.5% (after 2005). Our results demonstrate the importance of gender diversity in research collaborations and emphasize the need to increase the number of women in senior positions in medicine.

Keywords

Patent foramen ovale, Percutaneous PFO closure, Stroke, clinical study, human biology, randomized controlled trial (RCT), statistical power, medicine, Cochrane meta-analysis, human, meta research, mixed sex collaborations, General Immunology and Microbiology, General Biochemistry,Genetics and Molecular Biology, General Neuroscience

Citation

Otte, W M, Tijdink, J K, Weerheim, P L, Lamberink, H J & Vinkers, C 2018, 'Adequate statistical power in clinical trials is associated with the combination of a male first author and a female last author', eLife, vol. 7, e34412. https://doi.org/10.7554/eLife.34412