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临床试验/NCT00060086
NCT00060086已完成不适用

Phase II Study Evaluating Pomegranate Juice In Patients With Recurrent Adenocarcinoma Of The Prostate

Jonsson Comprehensive Cancer Center2 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2004年11月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
47
试验地点
2
主要终点
Clinical efficacy, in terms of overall response rate, measured by serum prostate-specific antigen (PSA) levels every 3 months

研究概览

简要总结

RATIONALE: Pomegranate juice may contain substances that decrease or slow the rise of prostate-specific antigen (PSA) levels and may be effective in delaying or preventing recurrent prostate cancer.

PURPOSE: This phase II trial is studying how well pomegranate juice works in decreasing or slowing the rise of PSA levels in patients who have undergone radiation therapy or surgery for prostate cancer.

详细描述

OBJECTIVES:

  • Determine whether pomegranate juice can decrease or slow rising prostate-specific antigen (PSA) levels in patients who have undergone radical prostatectomy or radiotherapy for adenocarcinoma of the prostate.

OUTLINE: Patients receive oral pomegranate juice once daily. Treatment continues for 18 months in the absence of disease progression or unacceptable toxicity.

PROJECTED ACCRUAL: A total of 29-40 patients will be accrued for this study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Histologically confirmed adenocarcinoma of the prostate
  • Must have undergone prior surgery or radiotherapy for the primary tumor
  • Documented rising prostate-specific antigen (PSA) level, defined by the following criteria:
  • Absolute level of PSA at least 0.2 ng/mL but less than 5.0 ng/mL
  • Rising PSA level must be confirmed at least 1 week later
  • Adequate PSA time points to calculate a PSA doubling time
  • Gleason score no greater than 7
  • Age 18 and over
  • Performance status ECOG 0-1
  • Life expectancy at least 6 months
  • No other malignancy within the past 5 years except nonmelanoma skin cancer
  • No other serious concurrent systemic medical disorders that would preclude study compliance
  • No known allergy to pomegranate juice
  • More than 4 weeks since prior participation in another experimental study

排除标准

  • nodal involvement
  • evidence of metastatic disease
  • prior hormonal therapy
  • concurrent hormonal therapy for rising PSA levels after initial therapy for prostate cancer
  • concurrent participation in another experimental study
  • other concurrent systemic or local therapy for prostate cancer
  • initiation or discontinuation of any new nutritional or dietary supplements during study participation

结局指标

主要结局

Clinical efficacy, in terms of overall response rate, measured by serum prostate-specific antigen (PSA) levels every 3 months

时间窗: Evaluated every 3 months for 18 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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