Editorial: Clinical trial design and development in neonatal and perinatal medicine

Editorial on the Research Topic
Clinical trial design and development in neonatal and perinatal medicine

Recent evidence from perinatal trials has significantly improved neonatal care, leading to a reduction in neonatal mortality, morbidity, and long-term disability. These advancements have integrated clinical trials into neonatal and perinatal practice and facilitated progress in the expanding Clinical Trial Design and Development field in Neonatal and Perinatal Medicine. Frontiers in Pediatrics has organized a series of Research Topics focused on clinical trials in Neonatal and Perinatal Medicine to highlight the latest advancements in this field. This editorial addresses new insights, novel developments, ongoing challenges, recent discoveries, and future perspectives in the field. This Research Topic aims to illuminate key advancements achieved over the past decade in Clinical Trials related to Neonatal and Perinatal Medicine. This Special Issue seeks to bridge the gap between research and clinical practice, fostering a deeper understanding of new possibilities and encouraging discussions within the perinatal and neonatal medicine communities. The thematic series covers various topics of interest to the perinatal and neonatal communities.

In the fields of pharmacokinetics and pharmacodynamics, Yeung et al. highlighted the principles and unique considerations for optimal design of neonatal clinical trials. Jilani et al., through a literature review applying the RAND/UCLA Appropriateness Method and thematic analysis, found that the interactional relationship between the opioid-exposed birthing person and the infant is the foundational principle that clinically defines the dyad to better support bedside care, surveillance, and research. Jumani et al. conducted a multicenter retrospective study to evaluate the short-term effects of opioids during therapeutic hypothermia (TH) for neonatal encephalopathy. Their study showed that opioid use during TH was associated with adverse short-term outcomes and highlighted the need for longer-term cohort studies. Köber et al. found that the gestational age at birth, birth weight, and gestational age at the time of intrauterine brain sparing determine neonatal outcomes in growth-restricted infants born before 32 weeks of gestation. Furthermore, a small subset of data showed that the nitric oxide donor pentaerythrityl tetranitrate (PETN) may ameliorate the effect of brain sparing in the affected neonates. The work of Pei and Chen explored the association between dexamethasone usage prior to elective full-term cesarean delivery and short-term adverse neonatal outcomes using a retrospective cohort study design. Their results suggest the importance of exercising caution when contemplating the use of antenatal corticosteroids-prior to elective full-term cesarean delivery. Allegaert et al. reported on the current status, trajectory, stakeholder assessment, impact, and future perspectives of the Neonatal Adverse Event Severity Scale (NAESS). This tool was developed by the International Neonatal Consortium (INC) to standardize assessment, facilitate reproducibility of results, and assess the severity and causality of adverse events in clinical trials.

Finally, Degl et al. provided the perspective of two parents of premature infants and two neonatal nurses on the partnership and strong bond that develops between parents and NICU nurses. With nurses being a constant calming presence at the bedside, a trusting bond between parents and nurses often helps to promote clinical research and becomes the lifeline to survive the NICU journey. Fully realizing this “bond” will improve outcomes for patients and families and contribute to the growth and success of the entire NICU system.

In conclusion, we hope that this collection of articles, which showcases a variety of complementary contributions from various institutions worldwide, will inform, guide, and inspire researchers in the field of perinatal and neonatal medicine and continue to lead to improvements in survival and outcomes.

Author contributions

MA-L: Conceptualization, Project administration, Resources, Supervision, Writing – original draft, Writing – review & editing. YK: Writing – review & editing. SU: Writing – review & editing. DB: Writing – review & editing. JD: Conceptualization, Project administration, Resources, Supervision, Validation, Writing – review & editing.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The author(s) declared that they were editorial board members of Frontiers at the time of submission. This had no impact on the peer review process and the final decision.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: trial, neonate, perinatal, design, studies

Citation: Abdel-Latif ME, Kandasamy Y, Uthaya S, Bassler D and Davis JM (2025) Editorial: Clinical trial design and development in neonatal and perinatal medicine. Front. Pediatr. 13:1557059. doi: 10.3389/fped.2025.1557059

Received: 7 January 2025; Accepted: 22 January 2025;
Published: 6 February 2025.

Edited and Reviewed by: David Warburton, Children's Hospital Los Angeles, United States

Copyright: © 2025 Abdel-Latif, Kandasamy, Uthaya, Bassler and Davis. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Mohamed E. Abdel-Latif, YWJkZWwtbGF0aWYubW9oYW1lZEBhY3QuZ292LmF1

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