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临床试验/NCT01758562
NCT01758562已完成不适用

Caphosol® Versus State-of-the-art Mouthcare in Patients With Allogeneic Stem Cell Transplantation: a Randomized Controlled Study About the Efficacy of the Mouth Rinse Caphosol®

University of Zurich1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2013年1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
已完成
入组人数
72
试验地点
1
主要终点
Duration of oral mucositis

研究概览

简要总结

Randomized controlled study about the efficacy of the mouth rinse Caphosol in patients with allogeneic stem cell transplantation. 85% of the patients receive a severe oral mucositis due to their treatment.

70 patients will be randomized in the intervention (Caphosol) or in the standard (state-of-the-art) group. Primary endpoint is the duration of the mucositis, secondary endpoints are the occurence of oral mucositis measured with the WHO-scale and the occurence of pain measured with the NRS-scale (Numeric Rating Scale).

  • Trial with medical device

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
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Allogeneic stem cell transplantation
  • •Male and female patients age 18-80
  • •Signed informed consent after information

排除标准

  • •Contra-indications due to ethical reasons
  • •Unable to read or write
  • •Unable to speak or understand the german language
  • •Low-salt diet

研究组 & 干预措施

State-of-the-art mouth care

No Intervention

Mouth rinse Caphosol

Active Comparator

Mouth rinse,aqueous solution. Caphosol is a preparation comprising two separately packaged aqueous solutions, a phosphate solution and a calcium solution, which, when both solutions are combined in equal volumes, forms a solution supersaturated with respect to both calcium and phosphate ions.

干预措施: Caphosol (Device)

结局指标

主要结局

Duration of oral mucositis

时间窗: 20-30 days

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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