Investigating started sample size, completed sample size and drop-out rate in 10 252 phase III clinical trials: Insights from ClinicalTrials.gov

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY British journal of clinical pharmacology Pub Date : 2025-02-20 DOI:10.1002/bcp.70023
Henian Chen, Jinyong Pang, Yayi Zhao, Biwei Cao, Matthew J. Valente, Weiliang Cen, Elena Valkanova
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Abstract

Aims

This study investigated the started sample size, completed sample size and drop-out rate of 10 252 published and unpublished phase III clinical trials registered on ClinicalTrials.gov over the past 20 years.

Methods

We conducted a comprehensive search on ClinicalTrials.gov for all phase III clinical trials with registered results before 26 May 2023. We retrieved and downloaded 10 252, which covered a period of more than 20 years.

Results

Out of the 10 252 trials analysed, 889 (8.7%) were sponsored by the US National Institutes of Health/US Federal agencies (NIH/US Fed), 8429 (82.2%) were sponsored by industry. The overall median started sample size was 302. The overall median completed sample size was 228. The median completed sample sizes were 258 for industry-sponsored trials, and 194 for NIH/US Fed-sponsored trials. The median completed sample sizes were 321 for biological interventions and 223 for drug interventions. The overall median drop-out rate was 11%. Statistically significant differences were observed in sample sizes between industry-sponsored trials and NIH/US Fed-sponsored trials (P < 0.0001). Neither the started sample sizes nor the completed sample sizes have shown any change over the course of the past 20 years.

Conclusions

Our findings indicate that a majority of the analysed trials lack sufficient statistical power (80%) to detect small effect sizes, and approximately half of the trials did not have 80% power to detect medium effect sizes. Notably, trials funded by NIH/US Fed exhibit significantly smaller sample sizes compared to trials sponsored by industry. When conducting sample size calculations for clinical trials, it is crucial to consider the anticipated effect size, variability and drop-out rate.

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调查10252个III期临床试验的开始样本量、完成样本量和退出率:来自ClinicalTrials.gov的见解。
目的:本研究调查了过去20年在ClinicalTrials.gov上注册的10252项已发表和未发表的III期临床试验的开始样本量、完成样本量和退出率。方法:我们对2023年5月26日之前注册结果的所有III期临床试验在ClinicalTrials.gov上进行了全面检索。我们检索并下载了10252篇,涵盖了20多年的时间。结果:在分析的10252项试验中,889项(8.7%)由美国国立卫生研究院/美国联邦机构(NIH/ Fed)赞助,8429项(82.2%)由企业赞助。总体中位数起始样本量为302。总体中位数完成样本量为228。工业赞助的试验中位完成样本量为258,NIH/ fed赞助的试验中位完成样本量为194。生物干预的中位完成样本量为321例,药物干预的中位完成样本量为223例。总体退学率中位数为11%。在行业资助的试验和NIH/美联储资助的试验之间,在样本量上观察到统计学上显著的差异(P结论:我们的研究结果表明,大多数分析的试验缺乏足够的统计能力(80%)来检测小效应量,大约一半的试验没有80%的统计能力来检测中等效应量。值得注意的是,与工业赞助的试验相比,由NIH/ Fed资助的试验的样本量要小得多。在进行临床试验的样本量计算时,考虑预期的效应量、变异性和退出率是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
8.80%
发文量
419
审稿时长
1 months
期刊介绍: Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.
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