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临床试验/NCT00494039
NCT00494039Unknown3 期

I-125 Versus Pd-103 for Low Risk Prostate Cancer

VA Puget Sound Health Care System2 个研究点 分布在 1 个国家目标入组 602 人开始时间: 1998年1月最近更新:
适应症

试验速览

阶段
3 期
入组人数
602
试验地点
2
主要终点
Cancer control (biochemical and survival)

研究概览

简要总结

Objective: To test the hypothesis that the shorter half-life of Pd-103 versus I-125, will increase the rate of tumor eradication.

Research design A total of 600 patients with AJC clinical stage T1c-T2a prostatic carcinoma (Gleason grade 2 to 6, PSA 4 to 10 ng/ml) will be randomized to implantation with I-125 (160 Gy) versus Pd-103 (115 Gy).

详细描述

Objective

To test the hypothesis that the shorter half-life of Pd-103 versus I-125, will increase the rate of tumor eradication.

Research design A total of 600 patients with AJC clinical stage T1c-T2a prostatic carcinoma (Gleason grade 2 to 6, PSA 4 to 10 ng/ml) will be randomized to implantation with I-125 (160 Gy) versus Pd-103 (115 Gy).

Methodology: Patients will be randomized by the method of random permuted blocks.

Cancer status will be monitored by serial serum PSA at 6, 12, 18 and 24 months and yearly thereafter. Treatment-related morbidity will be monitored by personal interview, using standard American Urologic Association and Radiation Therapy Oncology Group criteria at 1, 3, 6, 12 and 24 months. Patients with serum PSA above 1.0 ng/ml two years after treatment will be considered to have residual or recurrent cancer and to have failed therapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Males age 40-80
  • Gleason score 5-6

排除标准

  • Lymph node positive

结局指标

主要结局

Cancer control (biochemical and survival)

时间窗: final analysis 2008(?)

次要结局

未报告次要终点

研究者

申办方类型
Fed

研究点 (2)

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