Clinical Pharmacology Department, La Paz University Hospital, IdiPAZ, Madrid, Spain.
Pharmacology and Therapeutics Department, School of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.
Clin Transl Sci. 2023 Dec;16(12):2654-2664. doi: 10.1111/cts.13659. Epub 2023 Oct 27.
Effective participant recruitment is a critical challenge in clinical trials. Inadequate enrollment of participants can precipitate delays, escalated costs, and compromise scientific integrity. Despite its relevance, particularly during the early phases, it persists as an obstacle in the field of clinical research. The primary aim of this study was to analyze the recruitment rates of early-phase clinical trials and evaluate their potential associations with key trial characteristics. Using a descriptive and statistical analysis, a research study was conducted based on the early-phase trials registered at the European Clinical Trials Register (EU-CTR), spanning the timeframe from January 2017 to December 2021. Among the 194 trials examined, we found median recruitment rates of 68%. A more detailed exploration revealed a greater level of success in terms of recruitment achievement in pediatric trials when compared to trials involving adults, non-oncologic trials, or those also developed in non-European countries. It is important to underscore that only 69 trials out of the total managed to conclude recruitment, with the most prevalent reason for premature cessation being the presence of efficacy and safety issues or sponsor's strategy. This number can be greatly improved. Despite certain disparities observed in the information within EU-CTR, we have successfully determined the recruitment rates of the studies and established associations with some of the clinical trial characteristics analyzed. Owing to the inherent constraints of this study, further research is warranted to gain a comprehensive understanding of the intricate interplay between trial characteristics and their impact on recruitment rates in early-phase studies.
有效的参与者招募是临床试验中的一个关键挑战。参与者招募不足可能会导致延迟、成本增加,并损害科学的完整性。尽管这一点很重要,特别是在早期阶段,但它仍然是临床研究领域的一个障碍。本研究的主要目的是分析早期临床试验的招募率,并评估其与关键试验特征的潜在关联。本研究基于 2017 年 1 月至 2021 年 12 月在欧洲临床试验注册中心(EU-CTR)注册的早期阶段试验,采用描述性和统计分析方法进行。在检查的 194 项试验中,我们发现中位数招募率为 68%。更详细的探索表明,与涉及成人、非肿瘤学或也在非欧洲国家开发的试验相比,儿科试验在招募方面的成功率更高。重要的是要强调,在总共 194 项试验中,只有 69 项试验成功完成了招募,提前停止的最常见原因是疗效和安全性问题或赞助商的策略。这一数字可以大大提高。尽管在 EU-CTR 中的信息存在某些差异,但我们已经成功地确定了研究的招募率,并确定了与一些临床试验特征的关联。由于本研究的内在局限性,需要进一步的研究来全面了解试验特征之间的复杂相互作用及其对早期研究中招募率的影响。