跳至主要内容
临床试验/NCT02776800
NCT02776800撤回不适用

A Randomized, Controlled Study of Allevyn Life in the Management of Wounds in Home Health Care

Smith & Nephew, Inc.3 个研究点 分布在 1 个国家开始时间: 2016年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
3
主要终点
Number of home health clinician visits in each group

研究概览

简要总结

When elderly patients need help caring for wounds, physicians may refer patients to home health care providers. The home health provider sees the patient in the patient's home and assists the patient with wound care. Working with the patient's physician, the home health provider will use the appropriate wound covering ("dressing" or "bandage") to cover the wound. The goal of the home health provider is to ensure that the wound stays clean and progresses toward closure. The home health provider will conduct in-home patient visits at appropriate intervals to assess the status of the wound.

Extensive resources are required to see patients in their own homes. If a dressing could effectively manage wounds and allow longer time between in-home visits (without affecting patient safety or progress of the wound toward closure), then resources could be saved. Thus, newer dressings are designed for longer wear times, using advanced foam pads and adhesives that help keep the dressing in place. The hypothesis of this study is that the use of Allevyn Life will decrease the number of in-home visits by home health providers without sacrificing patient safety.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •The informed consent document must be read, signed, and dated by the subject or the subject's legally authorized representative before conducting any study procedures or exams.
  • •Subjects sixty-five (65) years of age or older. Subjects may be of either sex and of any race.
  • •Willing and able to allow home health clinician to conduct all required study visits.
  • •The subject (or caregiver) must be able to follow instructions, including the ability to have regular contact with the home health clinician between study visits.
  • •Are covered by traditional Medicare.
  • •Have a wound that is suitable for treatment with a foam dressing and can be appropriately covered by a single piece of ALLEVYN Life or the comparator dressing.
  • •At Screening, wound exudate must be moderate to heavy, as determined by the home health clinician.
  • •Target wound may be a trauma wound, chronic wound, or post-surgical wound.
  • •Wound care is the primary reason for the home health clinician visits and determines the frequency of home health visits. Subjects may have other comorbidities, but these cannot be the determining factor in scheduling the frequency of the home health visits.

排除标准

  • •Contraindications or hypersensitivity to the use of the study dressings or their components (e.g., adhesive)
  • •Any wound that requires an additional covering (e.g., compression dressing, cast, etc.) over the study dressing that prevents daily visualization of the dressing under study.
  • •Target wound that requires daily dressing changes due to topical wound treatment (e.g., daily applications of ointments, creams, etc.)
  • •Target wound and dressing that cannot be visualized by the subject or subject's caregiver.

研究组 & 干预措施

Foam Dressing

Other

Standard Care - Foam Dressing

干预措施: Foam dressing with an integrated adhesive border (Device)

Allevyn Life

Experimental

Foam Dressing

干预措施: Allevyn Life (Device)

结局指标

主要结局

Number of home health clinician visits in each group

时间窗: 60 days

次要结局

  • Home health provider time on-site(60 days)
  • Total cost of each treatment group(60 days)
  • Assess the Cardiff Wound Impact Schedule(60 days)
  • Number of visits required compared to number initially anticipated(60 days)
  • Average dressing wear time(60 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (3)

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