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临床试验/NCT01563679
NCT01563679已完成不适用

Prospective Analysis of Percutaneous Ablations for Cancer Treatment

Emory University1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2012年2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
26
试验地点
1
主要终点
Effect of percutaneous and transarterial treatments for cancer in quality of life

研究概览

简要总结

This is a study involving patients with cancer who are referred by their treating physician for percutaneous locoregional therapies.

Patient's clinical and radiology findings, pathology findings, survival, treatment responses, and complications after their locoregional therapy will be studied.

详细描述

The efficacy of the percutaneous and transarterial treatments for solid tumors will be studied. Prospective study on patients who receive percutaneous locoregional therapies, including radiofrequency ablation (RFA), cryoablation, microwave ablation, IRE and chemical ablation for treatment of cancer will be performed.

Preoperative clinic chart, procedure note, postoperative chart, pre- and post-operative CT, MRI or Ultrasound, angiographic findings, biopsy results and pathologic findings, will be reviewed. Patient survival, treatment responses, complications after the therapy will be collected from clinic visits and clinical encounters.

Patient overall performance status before and after procedures will be assessed using the Quality of Life questionnaire (SF-36™ Health Survey).

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

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

入选标准

  • 18yrs of age
  • Cancer diagnosis
  • Candidate for Locoregional therapy
  • Willingness to sign informed consent

排除标准

  • Unable to sign informed consent
  • Patients not eligible for locoregional therapies

结局指标

主要结局

Effect of percutaneous and transarterial treatments for cancer in quality of life

时间窗: 1 year

Patients will complete the QOL questionnare during their follow up visits after procedure. 1 month, 3 months, 6 months and 1 year.

次要结局

  • response rate to percutaneous and transarterial treatment for cancer(1 month, 3 months, 6 months, 1 year.)

研究者

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

Hyun Kevin Kim

Director of Interventional Radiology and Image-guided Medicine

Emory University

研究点 (1)

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