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临床试验/NCT02600156
NCT02600156已完成不适用

A Pilot Study to Evaluate Magnetic Resonance Thermal Image-Guided Focal Laser Ablation of Prostate Cancer Tumors

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2015年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
7
试验地点
1
主要终点
Success rate

研究概览

简要总结

The primary purpose of this study is to evaluate the feasibility and safety of MRI-guided focal laser ablation (Laser-Induced Interstitial Thermal Therapy, LITT) to treat low-risk native prostate cancer.

详细描述

The study is being done to evaluate the safety and effectiveness of Magnetic Resonance Imaging (MRI)-guided focal laser therapy with the Visualase Thermal Therapy System to treat low-risk prostate cancer tumors. Unlike surgery or radiotherapy which affects a large portion of the prostate or the entire organ, localized or focal therapy is intended to treat a small portion of tissue in which the cancer has been found by biopsy.

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
45 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
否

入选标准

  • •Male, 45 years of age or older.
  • •Diagnosis of prostate adenocarcinoma.
  • •Clinical stage T1c or T2a.
  • •Gleason score of 7 (3+4 or 4+3) or Intermediate risk Gleason 6
  • •PSA less than or equal to 20 ng/mL
  • •Three or fewer biopsy locations with prostate cancer which correlate with MRI findings.
  • •No lesion > or = 2cm
  • •One, two, or three tumor suspicious regions identified on multiparametric MRI
  • •No definite radiographic indication of extra-capsular extension.
  • •Estimated survival of 5 years or greater, as determined by treating physician.
  • •Tolerance for anesthesia/sedation.
  • •Ability to give informed consent.

排除标准

  • •Presence of any condition (e.g., metal implant, shrapnel) not compatible with MRI.
  • •History of other primary non-skin malignancy within previous three years.

研究组 & 干预措施

Single arm study

Experimental

MR guided focal laser ablation of prostate cancer using the Visualase Thermal Therapy System.

干预措施: Focal laser ablation of the prostate (Procedure)

结局指标

主要结局

Success rate

时间窗: 3 years

To evaluate the procedural success rate of using the MR-guided laser ablation to target, access, thermally monitor, and focally ablate MR-visible prostate cancer lesions.

Incidence of treatment emergent adverse events

时间窗: 3 years

To evaluate patient-related safety by monitoring short and long-term complications related to the procedure such as but not limited to incontinence, impotence, and urethral fistulas.

次要结局

  • Short- and mid-term ablative success(3 years)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

David A. Woodrum

David A. Woodrum, M.D., Ph.D.

Mayo Clinic

研究点 (1)

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