跳至主要内容
临床试验/NCT05641168
NCT05641168已完成不适用

A Pilot Evaluation Exploring New Adhesive Materials and Their Ability to Adhere to Abdominal and Peristomal Skin

Coloplast A/S1 个研究点 分布在 1 个国家目标入组 114 人开始时间: 2021年4月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Coloplast A/S
入组人数
114
试验地点
1
主要终点
Adherent area

研究概览

简要总结

The study investigates different adhesive materials on healthy and peristomal skin

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
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

入选标准

  • Has given written consent
  • Be at least 18 years of age and have full legal capacity
  • Have had a colostomy/ileostomy/urostomy for more than one year (for stoma patients) Have suitable peristomal skin area (assessed by investigator) (for stoma patients)

排除标准

  • Currently receiving or have within the past 2 months received radio- and/or chemotherapy
  • Currently receiving or have within the past month received topical steroid treatment in the abdominal skin area or systemic steroid (tablet/injection) treatment
  • Are pregnant or breastfeeding
  • Having dermatological problems in the abdominal area (assessed by investigator)
  • Participate in other clinical investigations. Exception: Participation in other Coloplast sponsored clinical investigations is accepted under the circumstances that the subject has paused the activities in the investigation and are otherwise complying with the inclusion and exclusion criteria of this protocol

研究组 & 干预措施

Ostomy Adhesive material

Experimental

Newly designed ostomy adhesive material

干预措施: Adhesive material (Other)

comparator adhesive material

Other

Adhesive material already on the market e.g adhesive material from SenSura Mio ostomy product

干预措施: Standard adhesive material (Other)

结局指标

主要结局

Adherent area

时间窗: At every material change throughout the study, an average of 1 week

Adherent area (assessed by photos of adhesive materials)

次要结局

未报告次要终点

研究者

发起方
Coloplast A/S
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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