跳至主要内容
临床试验/NCT01230515
NCT01230515已完成不适用

Opioid Titration in the Hospice Setting: Barriers Assessment and Modification of the Model Order Sheet and Protocol

Vanderbilt-Ingram Cancer Center1 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2006年1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
65
试验地点
1
主要终点
Adequate pain control

研究概览

简要总结

The purpose of this study is to modify the opioid titration order sheet to meet the needs of the outpatient hospice population and to conduct a pilot trial to assess feasibility, utility, and derive preliminary efficacy data.

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
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient eligibility includes:
  • Alive Hospice outpatient
  • Diagnosis of carcinoma
  • Pain requiring fixed dose opioids
  • Age > 21 years
  • Not pregnant or lactating
  • Willing and able to sign informed consent
  • Able to speak/comprehend English
  • Caregiver eligibility will include:
  • Caregiver for an Alive Hospice patient
  • Willing and able to sign informed consent
  • Able to speak/comprehend English
  • Hospice Staff eligibility will include:
  • Currently on staff at Alive Hospice
  • Willing and able to sign informed consent
  • Able to read/speak English.
  • Referring Physician eligibility will include:
  • Having recently referred patients to Alive Hospice
  • Willing and able to sign informed consent and able to read/speak English.

排除标准

  • patients < 21 years of age
  • pregnant or lactating
  • patients, caregiver and or Hospice staff that does not speak/comprehend English

结局指标

主要结局

Adequate pain control

时间窗: Until death.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Barbara Murphy, MD

Professor of Medicine; Director, Cancer Supportive Care Program; Director, Head and Neck Research Program; Medical Oncologist

Vanderbilt-Ingram Cancer Center

研究点 (1)

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