ACTRN12617000537358已完成3 期
Efficacy of Incontinence Associated Dermatitis Interventions for Critically Ill Patients in Intensive Care: the Distinct Pilot Randomised Control Trial.
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1) >17 years of age
- •2) Incontinent of urine and/or stool.
- •3) Predicted ICU length of stay (LOS) of at least 5 days
排除标准
- •2) Colorectal surgery resulting in a colostomy
- •3) Current pressure area ulcer/sore where the skin is affected by incontinence.
- •4) Current community-acquired IAD.
- •5) Continent of urine and faeces.
- •6) Have a dermatological disease (e.g. psoriasis, eczema) that is likely to interfere with the evaluation of the patient.
- •7) Presence of a fungal infection on the study area
- •8) Are currently enrolled in 3 non-intervention drug or device studies in the ICU research site
- •9) Currently participating in an investigational drug or device study.
- •10) The participant has a medical condition that in the opinion of the investigator would exclude him/her from participating in the study.
- •11) Hypersensitivity to CavilonTM Advanced Skin Protectant or its excipients.
研究者
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