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临床试验/NCT02261311
NCT02261311Unknown不适用

An Innovation During the Surgical Wait; Evaluation of the Opportunity for Intervention

Ottawa Hospital Research Institute1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2017年3月最近更新:
适应症

试验速览

阶段
不适用
入组人数
200
试验地点
1
主要终点
Quality of life

研究概览

简要总结

The investigators will compare the differences in the scores between the baseline questionnaire (at diagnosis) and the second questionnaire (at treatment) in the RADS II patients that enrolled in pre-treatment trials versus those that don't.

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
19 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • >18 years of age
  • Diagnosis of BI-RADS 4 and 5 (highly suspicious for carcinoma) on an initial imaging
  • >2cm area of disease
  • Provide informed consent

排除标准

  • Previous neo-adjuvant therapy
  • Patients with recurrent disease

结局指标

主要结局

Quality of life

时间窗: up to 6 weeks

To determine if there are improvements in the measurements of anxiety through quality of life questionnaires completed at 2 different time points when participating in a window of opportunity trial verses not participating in a window of opportunity trial.

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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