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临床试验/NCT03632980
NCT03632980Unknown不适用

Evaluation of a Dynamic Focusing Ultrasonic Transducer for High Intensity Focused Ultrasound (HIFU) Treatment of Localized Prostate Adenocarcinoma - Dose Escalation Trial to Define the Best Acoustic Parameters

EDAP TMS S.A.2 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2011年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
180
试验地点
2
主要终点
Necrosis measurement (immediate efficacy)

研究概览

简要总结

Define the best acoustic parameters for the dynamic focusing HIFU transducer in the treatment of localized Prostate 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
Treatment
盲法
None

入排标准

年龄范围
70 Years 至 —(Older Adult)
性别
Male
接受健康志愿者

入选标准

  • for primary care patients:
  • Age > 70 years
  • PSA < 15 ng/mL
  • 12 randomized biopsies
  • Gleason score ≤ 3+4
  • Normal anal and rectal anatomy
  • American Society of Anesthesiologists risk (ASA) 1 or 2

排除标准

  • for primary care patients:
  • T3 patients
  • American Society of Anesthesiologists risk (ASA) 3
  • Metastatic disease (Bone scan...)
  • Previous prostate cancer therapy
  • Distance between rectal mucosa and prostatic capsule of more than 8 mm thickness
  • Prostate volume over 50cc
  • Previous bladder cancer
  • contraindication to MRI
  • previous rectal or urinary fistulae
  • Inclusion Criteria for salvage patients:
  • Age > 50 years
  • Biochemical recurrence after radiotherapy (Phoenix definition: nadir+2ng/ml)
  • 12 randomized biopsies
  • Normal anal and rectal anatomy
  • ASA 1 or 2
  • Exclusion Criteria for salvage patients:
  • T3 patients
  • Metastatic disease (Bone scan...)
  • Distance between rectal mucosa and prostatic capsule of more than 8 mm thickness
  • Prostate volume over 50cc
  • Previous bladder cancer
  • contraindication to MRI
  • previous rectal or urinary fistulae

研究组 & 干预措施

HIFU prostate treatment

Experimental

The HIFU intervention will concern Primary care patients or Secondary care patients (salvage).

Intervention with "Ablatherm Foc/Dyn" or "Focal One" HIFU treatment devices

HIFU intervention will be administered with "Ablatherm Foc/Dyn or Focal One - First line" to Patients suffering from localized prostate cancer that has not been previously treated or Salvage HIFU intervention will be administered with "Ablatherm Foc/Dyn or Focal One - Post radiotherapy" to subjects harboring prostate cancer recurrency after radiotherapy

干预措施: "Ablatherm Foc/Dyn" or "Focal One" HIFU treatment (Device)

结局指标

主要结局

Necrosis measurement (immediate efficacy)

时间窗: Day 7

The coagulation necrosis induced by the HIFU dynamic focusing treatment of the prostate is evaluated by MRI in the first week post treatment.

次要结局

  • Adverse events reporting rates (safety and the morbidity) at 6 months(6 months)
  • Histological marker measurement (mid term efficacy)(6 months)
  • Biochemical marker measurement (mid term efficacy)(6 months)
  • Rectal wall preservation (immediate safety and morbidity)(Day 7)
  • Adverse events reporting rates (safety and the morbidity) at 24 months(24 months)
  • Quality of life score(6 months)
  • IPSS score(6 months)
  • IIEF-5 score(6 months)

研究者

发起方
EDAP TMS S.A.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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