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临床试验/CTIS2022-501892-14-00
CTIS2022-501892-14-00进行中(未招募)1 期

Evaluation of PSMA-PET and mpMRI in high-risk prostate cancer – using histopathologic validation - PAMP2

Region Vasterbotten0 个研究点目标入组 20 人开始时间: 2023年12月20日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
20

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 65+(—)
性别
Male

入选标准

  • Histologically confirmed high-risk prostate cancer planned to be treated with radical prostatectomy, PSMA-PET/CT conducted as part of the clinical management for the existing prostate cancer, =4 weeks since last biopsy of the prostate, One or more of the following criteria: a) cT3, or high suspicion of extra prostatic growth on mpMRI b) Gleason score =8 c) PSA 20-49 ng/ml, >18 years, Given a written consent to participate in the trial

排除标准

  • Non-MR-safe implants or another contraindication to MRI or PET, Tinnitus or severe hearing loss, Claustrophobia, Unfit for MRI or PET/MRI examination for any other reason, e.g., back pain, WHO PS >1, Patients treated with neoadjuvant/concomitant anti-testosterone treatment (surgical or medical castration such or anti-androgens), TUR-P within 6 months, Metastatic disease in skeleton, parenchymal organs, or lymph nodes outside the pelvis., Patients with previous diagnosis of other malignant disease. Exceptions could be made for basal cell carcinoma of the skin or progression free survival at least 10 years after any previous tumor., Creatinine clearance < 30ml/min

研究者

发起方
Region Vasterbotten

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