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23年儿科临床试验特征与活跃度分析——欧洲儿科法规对法国一家临床研究中心的影响

Analysis of Paediatric Clinical Trial Characteristics and Activity Over 23 Years-Impact of the European Paediatric Regulation on a Single French Clinical Research Center.

作者信息

Arnadottir Johanna, Luc François, Kaguelidou Florentia, Jacqz-Aigrain Evelyne

机构信息

Clinical Investigation Center CIC1426, Hôpital Robert Debré Assistance Publique-Hôpitaux de Paris INSERM, Paris, France.

Paris University, Paris, France.

出版信息

Front Pediatr. 2022 Apr 26;10:842480. doi: 10.3389/fped.2022.842480. eCollection 2022.

Abstract

As unlicensed or off-label drugs are frequently prescribed in children, the European Pediatric Regulation came into force in 2007 to improve the safe use of medicinal products in the pediatric population. This present report analyzes the pediatric research trials over 23 years in a clinical research center dedicated to children and the impact of regulation. The database of trial characteristics from 1998 to 2020 was analyzed. We also searched for differences between two periods (1998-2006 and 2007-2020) and between institutional and industrial sponsors during the whole period (1998-2020). A total of 379 pediatric trials were initiated at our center, corresponding to inclusion of 7955 subjects and 19448 on-site patient visits. The trials were predominantly drug evaluation trials ( = 278, 73%), sponsored by industries ( = 216, 57%) or government/non-profit institutions ( = 163, 43%). All age groups and most subspecialties were concerned. We noted an important and regular increase in the number of trials conducted over the years, with an increased number of multinational, industrially sponsored trials. Based on the data presented, areas of improvement are discussed: (1) following ethical and regulatory approval depending on the sponsor, the mean time needed for administrative and financial agreement, validation of trial procedures allowing trial initiation at the level of the center was 6.3 and 6.5 months (periods 1 and 2, respectively) and should be reduced, (2) availability of expert research teams remain insufficient, time dedicated to research attributed to physicians should be organized and recognition of research nurses is required. The positive impact of the European Pediatric Regulation highlights the need to increase the availability of trained research teams, organized within identified multicenter international pediatric research networks.

摘要

由于未获许可或未按说明书用药的情况在儿童中经常出现,2007年欧洲儿科法规生效,以提高药品在儿科人群中的安全使用。本报告分析了一个专门针对儿童的临床研究中心23年来的儿科研究试验以及法规的影响。对1998年至2020年的试验特征数据库进行了分析。我们还研究了两个时期(1998 - 2006年和2007 - 2020年)之间以及整个时期(1998 - 2020年)机构赞助商和行业赞助商之间的差异。我们中心共开展了379项儿科试验,纳入了7955名受试者,进行了19448次现场患者访视。这些试验主要是药物评估试验(n = 278,73%),由行业(n = 216,57%)或政府/非营利机构(n = 163,43%)赞助。所有年龄组和大多数亚专业都涉及到了。我们注意到这些年来进行的试验数量有显著且持续的增加,跨国的、由行业赞助的试验数量也有所增加。基于所呈现的数据,讨论了改进的方面:(1)根据赞助商的情况遵循伦理和监管批准,行政和财务协议、试验程序验证所需的平均时间(分别为时期1和时期2),这使得中心层面能够启动试验的时间分别为6.3个月和6.5个月,应予以缩短;(2)专家研究团队的可用性仍然不足,应组织分配给医生的研究时间,并需要认可研究护士。欧洲儿科法规的积极影响凸显了增加在已确定的多中心国际儿科研究网络内组建的训练有素的研究团队可用性的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eff5/9086591/2f4c7183f3b3/fped-10-842480-g001.jpg

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