Knöps Eva, Spuls Phyllis, Duijnhoven Ruben, Dijkgraaf Marcel, van Barreveld Marit, Arents Bernd, van Enst Annefloor, Garritsen Floor, Merkus Maruschka, Middelkamp-Hup Maritza Albertina, Musters Annelie, Bosma Angela, Hyseni Ariënna, Dijkstra Jitske, Hijnen Dirk Jan, Gerbens Louise
Department of Dermatology, Amsterdam UMC, Location Academic Medical Center, Amsterdam Public Health, Infection and Immunity, University of Amsterdam, Amsterdam, The Netherlands.
Department of Obstetrics and Gynecology, Amsterdam UMC, Amsterdam Reproduction & Development Research Institute, University of Amsterdam, Amsterdam, the Netherlands.
Trials. 2024 Jul 16;25(1):482. doi: 10.1186/s13063-024-08334-z.
Narrowband ultraviolet B (NB-UVB) phototherapy is commonly prescribed for patients with moderate-to-severe atopic eczema (AE). The efficacy of NB-UVB, however, has not yet properly been established, as current evidence is of low certainty. Our aim is to assess the short-term and long-term (cost-)effectiveness and safety of NB-UVB in adult AE patients by performing a pragmatic, multicenter, prospective, randomized, open-label, blinded-endpoint (PROBE) trial. This protocol outlines its methodology.
A pragmatic, multicenter, PROBE trial will be performed with 1:1 randomization of 316 adult patients with moderate-to-severe AE who have inadequate disease control with topical therapy and who are eligible for optimal topical therapy (OTT) or NB-UVB in combination with OTT as a next step. Participants in the interventional arm will receive a minimum of 3 months of OTT combined with 8 to 16 weeks of NB-UVB. The control group receives 3 months of OTT. Following the interventional phase, follow-up will continue for 9 months. Physician-reported and patient-reported outcomes (according to the Harmonising Outcome Measures for Eczema (HOME) Core Outcome Set) and adverse events are assessed at 4 weeks, 3, 6, 9, and 12 months.
The UPDATE trial aims to provide high-quality evidence regarding the (cost-)effectiveness and safety of NB-UVB phototherapy in moderate-to-severe AE patients. Challenges that are addressed in the protocol include the possible bias arising from applying open-label treatment and the necessity of introducing OTT into the study design to prevent a high dropout rate.
ClinicalTrials.gov NCT05704205. Registered on December 8, 2022.
窄谱中波紫外线(NB-UVB)光疗常用于中重度特应性皮炎(AE)患者。然而,由于目前证据的确定性较低,NB-UVB的疗效尚未得到充分证实。我们的目的是通过开展一项实用、多中心、前瞻性、随机、开放标签、盲终点(PROBE)试验,评估NB-UVB在成年AE患者中的短期和长期(成本)效益及安全性。本方案概述了其方法。
将进行一项实用、多中心的PROBE试验,对316例中重度AE成年患者按1:1随机分组,这些患者局部治疗疾病控制不佳,有资格接受最佳局部治疗(OTT)或NB-UVB联合OTT作为下一步治疗。干预组参与者将接受至少3个月的OTT联合8至16周的NB-UVB治疗。对照组接受3个月的OTT治疗。在干预阶段之后,随访将持续9个月。在第4周、3个月、6个月、9个月和12个月时评估医生报告和患者报告的结局(根据湿疹协调结局测量(HOME)核心结局集)以及不良事件。
UPDATE试验旨在提供关于NB-UVB光疗在中重度AE患者中的(成本)效益和安全性的高质量证据。本方案中解决的挑战包括应用开放标签治疗可能产生的偏倚,以及在研究设计中引入OTT以防止高脱落率的必要性。
ClinicalTrials.gov NCT05704205。于2022年12月8日注册。