跳至主要内容
临床试验/NCT02152020
NCT02152020已完成不适用

Patient-Centered Integration of Acupuncture to Decrease Pain for Cancer Survivors

Abramson Cancer Center at Penn Medicine1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2014年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
36
试验地点
1
主要终点
Number of Adverse Events

研究概览

简要总结

The objective of this study is to find out if acupuncture can improve the management of pain in cancer patients when used as part of a treatment plan that includes conventional pain medications. The investigators will enroll 36 cancer patients at Abramson Cancer Center and Penn Cancer Network sites. Participants will be enrolled in either the Conventional Pain Management group or Integrative Pain Management group.

研究设计

研究类型
Observational
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

  • Women or men age 18 years or older
  • Primary diagnosis of cancer with history of stage I, II, or III cancer
  • Finished primary cancer treatments (surgery, chemotherapy, radiotherapy)
  • Have a Karnofsky score of 60 or greater
  • Can understand written English
  • Have worst pain rated at least 4 or greater on an 11-point (0-10) numerical rating scale in the preceding week
  • Have been taking pain medications daily
  • Have had at least 15 days with pain in the preceding 30 days.

排除标准

  • Women or men with metastatic (stage IV) cancer
  • Unstable and progressive medical conditions as judged by the PIs or designated research nurse at the community hospitals (e.g., progressive cancer, uncontrolled heart failure) that may require hospitalization in the next 12 weeks
  • Planned surgical procedures in the next 12 weeks
  • Patients currently in a pain crisis as judged by the PI or designated research nurse that may warrant acute titration of medications or hospitalization
  • Women who are pregnant or breastfeeding
  • Unwillingness to adhere to study related procedures.

结局指标

主要结局

Number of Adverse Events

时间窗: 12 weeks

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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