A Clinical Evaluation of 3M Cavilon Advanced Barrier Film for the Treatment of Incontinence Associated Dermatitis (IAD)
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 16
- 主要终点
- Number of Participants With Change in Incontinence Associated Dermatitis Score
研究概览
简要总结
The purpose of this study is to obtain information concerning the safety and effective use of a protective barrier film in patients experiencing severe incontinence associated dermatitis.
详细描述
This is an open label, non randomized prospective case series evaluating 3M Cavilon Advanced Barrier Film for the treatment of severe incontinence associated dermatitis (IAD) in the presence or absence of continued fecal or fecal and urinary incontinence. The product will be applied twice a week for a maximum duration of 3 weeks. Subjects will be followed twice a week until healing, for a maximum of 3 weeks or earlier, if discharged from the facility. During the study period, the frequency and intensity of their incontinence will be monitored, twice a week photographic documentation and IAD site assessments will be completed.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Is the subject 18 years of age or older?
- •Is the subject in a facility providing nursing care 24h per day?
- •Does the subject have severe incontinence-associated dermatitis eg breached or denuded skin? The ideal candidate would have denudement present.
- •Is the subject willing to have photos taken of their skin exposed to incontinence and permit use of the photos in potential publications?
- •Is the subject willing to release rights to 3M for use of the photos?
- •Has the subject signed an Institutional Review Board-approved informed consent document and authorized the use and disclosure of protected health information? At NS-LIJ, only subjects who are capable of consenting are eligible to enroll. The study will not include participants with decisional impairment that would render them incapable of informed consent.
- •18 years or older
排除标准
- •Subjects are excluded from participation in this study if any of the answers to these questions is yes.
- •If female, is the subject pregnant or breast feeding or have they given birth within the 3 weeks preceding the screening visit?
- •Does the subject have a known allergy to acrylates or cyanoacrylate?
- •Does the subject have a current pressure ulcer in the area where the skin is affected by incontinence?
- •Does the subject have an active genital herpes infection?
- •Does the subject have a pre-existing abnormal skin disease on the treatment areas that may affect skin assessment?
- •Does the skin area involved in this study require treatment with a concomitant medication or product?
- •Has the subject been enrolled in any investigational study within 30 days of the Screening Visit?
- •Does the subject have any medical condition that in the opinion of the investigator should exclude him/her from participating in the study?
- •Has the subject received antifungal powders within 24 hours prior to enrollment?
- •Has the subject received cyanoacrylate based skin protectant to the affected areas (such as Marathon) within 72 hours prior to enrollment?
- •Is the facility unwilling to discontinue use for this subject of Dimethicone containing wipes on the area where the investigational device will be applied?
- •Is the facility unwilling to discontinue use for this subject of Chlorhexidine Gluconate wipes on the area where the investigational device will be applied?
研究组 & 干预措施
Cavilon Advanced Barrier Film
Cavilon Advanced Barrier Film applied to areas of IAD
干预措施: Cavilon Advanced Barrier Film (Device)
结局指标
主要结局
Number of Participants With Change in Incontinence Associated Dermatitis Score
时间窗: Baseline and end of treatment (up to 3 weeks)
Patients who were experiencing Incontinence Associated Dermatitis (IAD) from exposure to urine, stool or a combination of both urine \& stool received an application of the barrier film every 72 hours. A skin assessment tool designed for IAD was used to document each patient's IAD score over time. The area scored was divided into 6 zones, l \& r buttocks, L \& right thighs, perianal \& gluteal cleft. The % area within each zone with denudement was X by 9, redness was X by 3 and healthy skin X 1. The total score range of the 6 zones was 0-3654 with 3654 being worst case scenario. Improvement of IAD Score - At baseline (enrollment) the six zones were evaluated for % of denudement, redness, pink and healthy skin assessed. At the end of subject's participation, assessment were completed again to determine final score \& change for improvement was measured by reduction in IAD score No improvement of IAD score - No change in score Progression of IAD score - Increase in IAD score
次要结局
未报告次要终点