Effectiveness of a Burnaid® hydrogel dressing in Reducing Pain in Children Within the Early Management of the Acute Paediatric Burn; a Randomised Controlled Trial

ady Cilento Children's Hospital0 个研究点目标入组 72 人开始时间: 2017年9月5日最近更新: 2021年11月8日

适应症

试验速览

暂无简介。

•Children recruited into the study will age between 0 – 16 years that have acquired an acute thermal burn injury that is below 20% of the Total Body Surface Area (TBSA). The child must present to the emergency department or burns outpatient department within 24 hours of sustaining the injury, and have no silver dressing application prior to this admission.

•Children outside of the age group will be excluded from the study along with if their mechanism is on e of the following causes; chemical, electrical, inhalation, or friction; children who do not arrive within 24 hours of sustaining their acute burn injury; children who received prior treatment of a silver dressing; are non English speaking; children with cognitive impairments; ventilated or require initial wound care in theatre for debridement or grafting; current involvement with the Department of Communities (child safety); have co-morbidities that would potentially impair would healing (e.g. diabetes) or that may exacerbate itch and pain. Apart from which type of dressing the child is receiving prior to the application of silver, all participants will receive the standard medical care as would those not in the trial.

发起方

ady Cilento Children's Hospital