Department of Laboratory Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK
Edinburgh Clinical Research Facility, The University of Edinburgh, Edinburgh, UK.
BMJ Open. 2021 May 5;11(5):e049964. doi: 10.1136/bmjopen-2021-049964.
Edinburgh and Lothians' Viral Intervention Study Kids is a parallel, open-label, randomised controlled trial of hypertonic saline (HS) nose drops (~2.6% sodium chloride) vs standard care in children <7 years of age with symptoms of an upper respiratory tract infection (URTI).
Children are recruited prior to URTI or within 48 hours of developing URTI symptoms by advertising in areas such as local schools/nurseries, health centres/hospitals, recreational facilities, public events, workplaces, local/social media. Willing parents/guardians, of children <7 years of age will be asked to contact the research team at their local site. Children will be randomised to either a control arm (standard symptomatic care), or intervention arm (three drops/nostril of HS, at least four times a day, until 24 hours after asymptomatic or a maximum of 28 days). All participants are requested to provide a nasal swab at the start of the study (intervention arm: before HS drops) and then daily for four more days. Parent/guardian complete a validated daily diary, an end of illness diary, a satisfaction questionnaire and a wheeze questionnaire (day 28). The parent/guardian of a child in the intervention arm is taught to prepare HS nose drops. Parent/guardian of children asymptomatic at recruitment are requested to inform the research team within 48 hours of their child developing an URTI and follow the instructions already provided. The day 28 questionnaire determines if the child experienced a wheeze following illness. Participation in the study ends on day 28.
The study has been approved by the West of Scotland Research Ethics Service (18/WS/0080). It is cosponsored by Academic and Clinical Central Office for Research and Development-a partnership between the University of Edinburgh and National Health Service Lothian Health Board. The findings will be disseminated through peer-reviewed publications, conference presentations and via the study website.
NCT03463694.
爱丁堡和洛锡安病毒干预研究儿童是一项平行、开放标签、随机对照试验,比较高渗盐水(HS)滴鼻剂(~2.6%氯化钠)与标准护理在 7 岁以下有上呼吸道感染(URTI)症状的儿童中的疗效。
通过在当地学校/幼儿园、保健中心/医院、娱乐设施、公共活动、工作场所、当地/社交媒体等地方做广告,在 URTI 之前或出现 URTI 症状后 48 小时内招募儿童。愿意的父母/监护人,年龄在 7 岁以下的儿童,将被要求与当地研究小组联系。儿童将被随机分配到对照组(标准对症治疗)或干预组(每侧鼻孔滴 3 滴 HS,每天至少 4 次,直至无症状后 24 小时或最多 28 天)。所有参与者在研究开始时(干预组:在 HS 滴注之前)提供一个鼻腔拭子,然后在接下来的 4 天每天提供一个。家长/监护人填写一份经过验证的日常日记、疾病结束日记、满意度问卷和哮喘问卷(第 28 天)。干预组中儿童的家长/监护人在接受 HS 滴鼻剂治疗前被教授如何准备 HS 滴鼻剂。在招募时无症状的儿童的家长/监护人被要求在其孩子出现 URTI 后 48 小时内通知研究小组,并按照已经提供的说明进行操作。第 28 天的问卷确定孩子在患病后是否出现喘息。研究的参与在第 28 天结束。
该研究已获得西苏格兰研究伦理服务中心的批准(18/WS/0080)。它由爱丁堡大学和国民保健制度洛锡安卫生局之间的学术和临床中央研究与发展办公室共同赞助。研究结果将通过同行评审的出版物、会议演讲和研究网站传播。
NCT03463694。