Reinaud Camille, Mavoungou Sandra, Hajage David, Lieng Chloé, Rajendrabose Deivanes, Ferreira Diane, Blanchard Jules, Turpin Agathe, Dechartres Agnès
Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, Département de Santé Publique, Centre de Pharmacoépidémiologie de l'AP-HP (Cephepi), Paris, France.
JAMA Netw Open. 2025 Apr 1;8(4):e253569. doi: 10.1001/jamanetworkopen.2025.3569.
The noninferiority margin is a key methodological parameter in noninferiority trials that affects both sample size calculation and interpretation of results.
To assess (1) the reporting of the noninferiority margin on ClinicalTrials.gov, including when it was reported; (2) the consistency of the noninferiority margin between registration and publication; and (3) the reporting of the noninferiority margin at registration in a sample of recent trials.
This systematic review was conducted in 2 stages. Stage 1 involved identifying all noninferiority trials registered on ClinicalTrials.gov with a primary completion date of January 1, 2010, to January 1, 2015, and searching for corresponding publications. Stage 2 included all noninferiority trials registered between January 1, 2022, and June 30, 2023. Two reviewers independently and manually extracted methodological characteristics related to the noninferiority design for each trial at registration and, when available, in results posted on ClinicalTrials.gov and in publications. The time points for reporting the noninferiority margin were at registration, during the patient enrollment phase (between start date and primary completion date), after the primary completion date, or in results posted.
Among the 266 trials completed between 2010 and 2015, only 8 (3.0%) reported the noninferiority margin at registration. The noninferiority margin was reported after registration for 31 of 266 trials (11.7%), with 11 (4.1%) reporting it during the patient enrollment phase and 20 (7.5%) reporting it after the primary completion date. Of the 132 trials with results posted on ClinicalTrials.gov, 79 (59.8%) reported the noninferiority margin. A corresponding publication was found for 208 trials, with 196 (94.2%) reporting the noninferiority margin. For 5 trials reporting the margin at both registration and in publication, the noninferiority margin was consistent in both sources. Among the 327 noninferiority trials first posted between 2022 and 2023, 30 (9.2%) reported the noninferiority margin at registration.
In this systematic review, the reporting of the noninferiority margin on ClinicalTrials.gov was low. Mandatory reporting of the design and the noninferiority margin at registration could enhance the transparency and favor more reliable results.
非劣效界值是非劣效性试验中的一个关键方法学参数,它影响样本量计算和结果解读。
评估(1)ClinicalTrials.gov上非劣效界值的报告情况,包括报告时间;(2)注册时与发表时非劣效界值的一致性;(3)近期试验样本中注册时非劣效界值的报告情况。
本系统评价分两个阶段进行。第一阶段涉及识别在ClinicalTrials.gov上注册的所有主要完成日期为2010年1月1日至2015年1月1日的非劣效性试验,并搜索相应的出版物。第二阶段包括2022年1月1日至2023年6月30日期间注册的所有非劣效性试验。两名评审员独立且人工提取每个试验在注册时以及(如有)ClinicalTrials.gov上发布的结果和出版物中与非劣效性设计相关的方法学特征。报告非劣效界值的时间点为注册时、患者入组阶段(开始日期至主要完成日期之间)、主要完成日期之后或发布的结果中。
在2010年至2015年完成的266项试验中,只有8项(3.0%)在注册时报告了非劣效界值。266项试验中有31项(11.7%)在注册后报告了非劣效界值,其中11项(4.1%)在患者入组阶段报告,20项(7.5%)在主要完成日期之后报告。在ClinicalTrials.gov上发布结果的132项试验中,79项(59.8%)报告了非劣效界值。为208项试验找到了相应的出版物,其中196项(94.2%)报告了非劣效界值。对于5项在注册和发表时均报告了该界值的试验,两个来源的非劣效界值一致。在2022年至2023年首次发布的327项非劣效性试验中,30项(9.2%)在注册时报告了非劣效界值。
在本系统评价中,ClinicalTrials.gov上非劣效界值的报告率较低。强制要求在注册时报告设计和非劣效界值可提高透明度并有助于获得更可靠的结果。