跳至主要内容
临床试验/NCT01698645
NCT01698645Unknown不适用

A Spanish , Multicentre, Open-label, Observational Study to Assess Quality of Life and Satisfaction in Subjects Taking PecFent® for the Treatment of Breakthrough Cancer Pain (BTPc)

Archimedes Development Ltd1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2012年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
150
试验地点
1
主要终点
Satisfaction

研究概览

简要总结

National multicenter, prospective, observational study in cancer patients with chronic background pain and breakthrough pain to whom PecFent® has been prescribed under pragmatic condition by a specialist in the treatment of cancer pain conditions.

• Study objectives include assessment of early treatment satisfaction.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Adult (aged ≥18 years) with cancer
  • Taking at least 60 mg of oral morphine sulfate or equivalent per day for chronic background pain

排除标准

  • 未提供

研究组 & 干预措施

PecFent®

干预措施: PecFent® (fentanyl) nasal spray (Drug)

结局指标

主要结局

Satisfaction

时间窗: Satisfaction will be assessed approximately 1 hour after each breakthrough pain (BTPc) episode treated with PecFent® from completion of titration through Day 7

Satisfaction will be assessed using a 4-point Likert scale.

次要结局

未报告次要终点

研究者

发起方
Archimedes Development Ltd
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验