Division of Reproductive, Child Health and Nutrition (RCN), Indian Council of Medical Research (ICMR) Headquarters, V Ramalingaswami Bhawan, Ansari Nagar, New Delhi, Delhi, 110029, India.
Department of Community Medicine, Dr. Sushila Nayar School of Public Health, Mahatma Gandhi Institute of Medical Sciences (MGIMS), Sewagram, Wardha, Maharashtra, 442102, India.
Trials. 2024 Jul 5;25(1):458. doi: 10.1186/s13063-024-08298-0.
Despite progress in reducing the infant mortality in India, the neonatal mortality decline has been slower, necessitating concerted efforts to achieve Sustainable Development Goal-3. A promising strategy aiming to prevent neonatal sepsis in high-risk, vulnerable, low birth weight neonates through an innovative intervention includes probiotic supplementation. This article communicates the decision by the ProSPoNS trial investigators to establish a Central Endpoint Adjudication Committee (CEAC) as an addendum to the protocol published in Trials in 2021 for the purpose of clarifying the primary outcome. In the published protocol, the study hypothesis and primary objective are based on "sepsis," the primary outcome has been specified as sepsis/PSBI, whereas the sample size estimation was performed based on the "physician diagnosed sepsis." To align all the three above, the investigators meeting, held on 17th-18th August 2023, at MGIMS Sevagram, Wardha, deliberated and unanimously agreed that "physician diagnosed sepsis" is the primary study outcome which includes sepsis/PSBI. The CEAC, chaired by an external subject expert and members including trial statistician, a microbiologist, and all site principal investigators will employ four criteria to determine "physician diagnosed sepsis": (1) blood culture status, (2) sepsis screen status, (3) PSBI/non-PSBI signs and symptoms, and (4) the clinical course for each sickness event. Importantly, this clarification maintains consistency with the approved study protocol (Protocol No. 5/7/915/2012 version 3.1 dated 14 Feb 2020), emphasizing the commitment to methodological transparency and adherence to predefined standards. The decision to utilize the guidance of a CEAC is recommended as the gold standard in multicentric complex clinical trials to achieve consistency and accuracy in assessment of outcomes.Trial registrationClinical Trial Registry of India (CTRI) CTRI/2019/05/019197. Registered on 16 May 2019.
尽管印度在降低婴儿死亡率方面取得了进展,但新生儿死亡率的下降速度较慢,因此需要齐心协力实现可持续发展目标 3。一项有希望的策略是通过创新干预措施,为高风险、脆弱、低出生体重的新生儿补充益生菌,以预防新生儿败血症。本文传达了 ProSPoNS 试验的研究者决定成立一个中央终点裁决委员会(CEAC)的决定,作为 2021 年在 Trials 上发表的方案的附录,目的是澄清主要结局。在已发表的方案中,研究假设和主要目的是基于“败血症”,主要结局已指定为败血症/PSBI,而样本量估计是基于“医生诊断的败血症”进行的。为了使上述三个方面保持一致,于 2023 年 8 月 17 日至 18 日在沃德哈的 MGIMS Sevagram 举行的研究者会议上,经过审议,一致认为“医生诊断的败血症”是主要研究结局,包括败血症/PSBI。CEAC 将由一名外部主题专家担任主席,成员包括试验统计学家、微生物学家和所有现场主要研究者,将采用四项标准来确定“医生诊断的败血症”:(1)血培养状态,(2)败血症筛查状态,(3)PSBI/非 PSBI 体征和症状,以及(4)每个疾病事件的临床过程。重要的是,这一澄清与批准的研究方案(方案编号 5/7/915/2012,版本 3.1,日期为 2020 年 2 月 14 日)保持一致,强调了对方法透明性和遵守既定标准的承诺。建议使用 CEAC 的指导作为多中心复杂临床试验的金标准,以实现结局评估的一致性和准确性。
试验注册印度临床试验注册中心(CTRI)CTRI/2019/05/019197。于 2019 年 5 月 16 日注册。