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临床试验/EUCTR2019-004045-33-NL
EUCTR2019-004045-33-NL进行中(未招募)1 期

PredicTive value of FluoR-18 PSMA-1007 PET/CT and anti-3-[18F] FACBC PET/CT before PLND for lymph nodE staging in primary pRostate cancer - TRACER

Catharina Hospital Eindhoven0 个研究点目标入组 70 人开始时间: 2020年9月7日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Male

入选标准

  • 1. Biopsy proven adenocarcinoma of the prostate;
  • 2. Indication for (super)extended PLND (with or without (robot-assisted) laparoscopic prostatectomy), in intermediate and high risk patients ( d’Ámico score) with an MSKCC >5% lymph node prediction;
  • 3. Mentally competent and understanding of benefits and potential burden of the study;
  • 4. Written informed consent;
  • 5. Age =18 years.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 35
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 35

排除标准

  • 1. History of prior diagnosed or treated PCa.
  • 2. Known concomitant malignancies (except Basal Cell Carcinoma of the skin).
  • 3. Unwillingness or inability to undergo 18F-PSMA-1007 PET/CT and anti-3-[18F] FACBC PET/CT, in combination with PLND.
  • 4. Metastasis beyond pelvic region and/or bone metastasis. Patients with bone metastasis will not get a PLND, but will be included in the study for further follow-up.

研究者

发起方
Catharina Hospital Eindhoven

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