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临床试验/NCT01062100
NCT01062100已完成不适用

The Hamilton Prospective Pilot Study To Investigate the Feasibility and Safety of A Dedicated High Resolution Nuclear Breast Imaging Camera

Ontario Clinical Oncology Group (OCOG)1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2010年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
42
试验地点
1
主要终点
To assess the feasibility, safety and acceptability to patients of the MBI Gamma camera.

研究概览

简要总结

To evaluate the feasibility, acceptability and safety of using a molecular breast imaging (MBI) Gamma Camera in women at high risk of developing breast cancer

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Females ≥18 years of age
  • Undergoing annual breast MRI because of a high risk of breast cancer due to any of the following:
  • Known BRCA1 or BRCA2 mutation carriers, or is untested for BRCA but is a first degree relative of a BRCA mutation carrier
  • History of radiation to the chest between 10-30 years of age (e.g. Hodgkin's Disease)
  • History of Cowdens or Li Fraumeni Syndrome
  • A first degree relative with Cowdens or Li Fraumeni Syndrome
  • Prior breast biopsy positive for lobular carcinoma in situ (LCIS) or atypical lobular hyperplasia or atypical ductal hyperplasia (ADH)
  • Family history consistent with a hereditary breast cancer syndrome and estimated personal lifetime cancer risk ≥25% using the IBIS risk evaluator

排除标准

  • Pregnant or lactating
  • History of invasive breast cancer or ductal carcinoma in situ (DCIS)
  • Unable to undergo MRI because of:
  • Renal dysfunction with an estimated creatinine clearance of < 30 ml/min calculated using the Cockcroft-Gault formula
  • Implanted ferrous metal prostheses
  • Claustrophobia
  • Medical or psychological conditions that on assessment, make them unable to complete the procedure
  • Known allergies to Gadolinium-DTPA
  • Known allergies to Sestamibi (Miraluma or Cardiolite)
  • Prior bilateral mastectomy
  • Prior breast biopsy or surgery within 3 months

结局指标

主要结局

To assess the feasibility, safety and acceptability to patients of the MBI Gamma camera.

时间窗: 1 year

次要结局

  • To explore the ability of the MBI Gamma camera to detect breast cancer.(1 year)

研究者

发起方
Ontario Clinical Oncology Group (OCOG)
申办方类型
Other
责任方
Sponsor

研究点 (1)

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