NCT02094950已完成1 期
Acupuncture Feasibility Trial for Dyspnea in Lung Cancer
适应症
干预措施
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 12
- 试验地点
- 2
- 主要终点
- Dyspnea
研究概览
简要总结
This is a single arm clinical trial to establish the feasibility of conducting a clinical trial of acupuncture in reducing dyspnea among lung cancer survivors who have completed chemoradiotherapy. Twelve subjects with dyspnea will be recruited to this clinical trial. Up to 10 sessions of acupuncture will be delivered over the course of 8-10 weeks. The primary outcome will be dyspnea as measured by the English version of the Cancer Dyspnea Scale at the completion of the intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of Lung Cancer (Non small cell and small cell both eligible)
- •Completion of concurrent CRT at least 6 months prior to randomization.
- •Dyspnea which worsened after Chemoradiotherapy, leading to a ATS dyspnea score greater than or equal to 2 (Walks slower than people of the same age on the level because of breathlessness or has to stop for breath when walking at own pace on level)
- •Ability to understand written English -Willingness to adhere to all study-related procedures
- •Age 18 years old
- •ECOG Performance Status 1-3
排除标准
- •Current receipt of therapy for treatment related pneumonitis for 3 weeks.
- •Surgical resection of this LC (lobectomy or pneumonectomy)
- •Another organic cause of dyspnea necessitating treatment (eg pleural effusion appropriate for thoracentesis, rapidly progressive intrathoracic recurrence, symptomatic pulmonary embolus after CRT, untreated anemia with hemoglobin8 g/dL)
- •Current bleeding disorder by history
- •Life expectancy of 12 weeks, as assessed by primary oncologist
研究组 & 干预措施
Lung Cancer Patient with Dyspnea
Experimental
干预措施: Acupuncture (Procedure)
结局指标
主要结局
Dyspnea
时间窗: 10 weeks
次要结局
未报告次要终点
研究者
研究点 (2)
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