NCT05744557终止不适用
Vapocoolant Analgesia for Breast Lymphoscintigraphy
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 30
- 试验地点
- 2
- 主要终点
- Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
研究概览
简要总结
To learn if applying vapocoolant anesthetic spray ("Nüm") on the surface of the intended injection site will reduce the pain/anxiety associated with breast injections.
详细描述
Primary Objectives:
- Establish feasibility of topical vapocoolant in the setting of breast lymphoscintigraphy.
- Demonstrate safety of topical vapocoolant in the setting of breast lymphoscintigraphy.
Secondary Objectives:
- To assess patient pain intensity associated with the performance of breast lymphoscintigraphy.
- To evaluate the attitude from patients about supporting the continued offering of topical vapocoolant in the breast lymphoscintigraphy clinic.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
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
- •Any adult patient undergoing asubareolar breast lymphoscintigraphy injection will be eligible.
- •Age ≥18 years old
- •Ability to understand and the willingness to sign a written informed consent document.
- •Childbearing potential, lactating, pregnant women will be included.
排除标准
- •Patients who have allergy or had prior hypersensitivity to either of the vapocoolants including 1,1,1,3,3 Pentafluoropropane and 1,1,1,2-Tetrafluoroethane.
- •Patients with uncontrolled intercurrent illness (insulin dependent and non-insulin dependent diabetes)
- •Patients with psychiatric illness/social situations that would limit compliance with study requirements.
结局指标
主要结局
Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0
时间窗: through study completion; an average of 1 year.
次要结局
未报告次要终点
研究者
研究点 (2)
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