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临床试验/NCT05763355
NCT05763355
已完成
不适用

Multicentric Comparative Prospective Study of the Benefits and Risks of Biopsy Prostate Using Transrectal or Transperineal Procedure for the Prostate Cancer Diagnostic.

Elsan4 个研究点 分布在 1 个国家目标入组 101 人2023年12月15日

概览

阶段
不适用
干预措施
Biopsy
疾病 / 适应症
Patients With Suspected Prostate Cancer
发起方
Elsan
入组人数
101
试验地点
4
主要终点
Comparison of the rate of occurrence of biopsy-induced infection in both groups
状态
已完成
最后更新
9天前

概览

简要总结

The performance of prostatic biopsies is an essential element to confirm the diagnosis of prostate cancer and to specify the characteristics of the tumor in terms of stage and grade.

The first route of prostatic biopsies is mainly transrectal with passage of a needle introduced into the guide fixed on the endorectal ultrasound probe. There is another possible access route, transperineal, with prostatic puncture by a needle introduced transcutaneously, guided by an endorectal ultrasound image. The first transperineal route would offer the first benefit for the patient, to reduce the infectious risk inherent in the endorectal way. It would also reduce the risk of rectal bleeding.

In addition, the transperineal pathway appears to be able to improve the detection threshold of prostatic tumours located on the anterior part of the gland due to the angle of penetration of the needle and its more anterior positioning relative to the prostate.

There is currently no randomized comparison study of the transperineal versus transrectal procedure on infectious risk. The aim of the project is to enable this comparative study, within our institution where experienced urologist surgeons practice.

注册库
clinicaltrials.gov
开始日期
2023年12月15日
结束日期
2025年9月2日
最后更新
9天前
研究类型
Interventional
研究设计
Parallel
性别
Male

研究者

发起方
Elsan
责任方
Sponsor

入排标准

入选标准

  • Patients with suspected prostate cancer with at least one of the following criteria met :
  • MRI Staging: T2 or T3a,
  • MRI Grading: Pirads greater than or equal to 3
  • MRI tumor volume greater than or equal to 0.5 cm3
  • e.Patient without tumor lesion detected by prostate MRI less than 3 months old with PSA \> 4 ng/ml, or an observed suspicious induration to the rectal exam
  • Voluntarily signed and dated written informed consents prior to any study specific procedure,

排除标准

  • Other medical conditions may interfere with the conduct of the study and, in the judgment of the investigator, would make the patient inappropriate for entry into this study,
  • Individuals deprived of liberty or placed under legal guardianship,
  • Unwillingness or inability to comply with the study protocol for any reason.
  • Patients without a health insurance

研究组 & 干预措施

Transrectal biopsy using KOELIS fusion system

Transrectal procedure will be performed with the patient in the left lateral position with a completely free-hand technique utilising the KOELIS fusion system.

干预措施: Biopsy

Transperineal biopsy using KOELIS perine grid

Transperineal biopsy will be performed in the lithotomy position. KOELIS "Perine Grid" needle guidance device and "Steady Pro" free-hand probe arm will be utilised (free-hand assisted technique).

干预措施: Biopsy

结局指标

主要结局

Comparison of the rate of occurrence of biopsy-induced infection in both groups

时间窗: 30 days after intervention

Biopsy-induced infection are defined as : * Positive post-biopsy urinary test result * Clinical infection syndrome (T\>37.5°C fever) * Signs of urogenital infection (cystitis/prostatitis/orchi-epididymitis) * Hospitalization for hyperpyrexia * Septic shock

次要结局

  • Comparison of the rate of urethral bleeding (hematuria and urethrorrhagia) in both groups(30 days after intervention)
  • Comparison of the Percentage of underestimation of the stage of tumor development in both groups(3 months after intervention)
  • Comparison of the Procedure Time in both groups(1 day)
  • Comparison of the Room occupancy time in both groups(1 day)
  • Comparison of the rate of rectal bleeding in both groups(30 days after intervention)
  • Comparison of the percentage of negative biopsies in both groups(30 days after intervention)
  • Comparison of the percentage of positive biopsies on on anterior areas in both groups(30 days after intervention)
  • Comparison of the Average Length of Stay in both groups(1 day)
  • Assess the pain (tolerance) felt by the patient according to the biopsy method used(1 day)

研究点 (4)

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