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临床试验/NL-OMON44447
NL-OMON44447招募中不适用

Multi-center MRI-guided focal laser ablation of prostate cancer. - MRI-guided focal laser ablation

Radboud Universitair Medisch Centrum0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
25

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. MRI visible index lesion (on T2-weighted MR imaging or diffusion weighted imaging)
  • 2. maximum MRI visible lesion size is <<= 15 mm large axis
  • 3. 45 to 76 years old patient
  • 4. life expectancy at the inclusion of more 10 years
  • 5. underwent systematic TRUS-guided biopsy
  • 6. diagnosis of prostate cancer confirmed by targeted biopsy using TRUS-MRI fusion or in-bore
  • MRI guided biopsies
  • 7. criteria of low and intermediate risk of progression and eligibility for focal therapy
  • a. a clinical stage of maximum T2c
  • b. a maximum biopsy Gleason score of 4 + 3 on targeted biopsies
  • c. a serum prostate specific antigen < 15 ng/ml
  • 8. patient accepting to be included in an active surveillance protocol at the end of the study, in
  • accordance with the recommendations of good practice

排除标准

  • 1. history of prostate surgery
  • 2. history of radiation therapy or pelvic trauma; history of proved acute or chronic prostatitis
  • 3. history of tumor in the preceding 5 years (excluded: non-metastatic basal cell skin cancer)
  • 4. severe urinary symptoms associated with benign hyperplasia of the prostate, and defined by an
  • IPSS score > 18
  • 5. tumor with MRI signs of extra-capsular extension or invasion of the seminal vesicles
  • 6. maximum cancer core length >3 mm and/or maximum Gleason score of 3+4 on systematic
  • biopsies outside the visible tumor area on mpMRI
  • 7. Impossibility to obtain a valid informed consent
  • 8. Patients unable to undergo MR imaging, including those with contra-indications
  • 9. Contra-indications to MR guided focal laser therapy (colitis ulcerosa, rectal pathology or
  • abdomino perineal resection)
  • 10. Metallic hip implant or any other metallic implant or device that distorts local magnetic field and
  • compromises the quality of MR imaging
  • 11. Patients with evidence for nodal or metastatic disease
  • 12. Patients with an estimated Glomerular Filtration Ratio (eGFR) < 40 mL/min/1.73 m2

研究者

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