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临床试验/ACTRN12612000101886
ACTRN12612000101886已完成1 期

A Randomized controled trial of Famotidine as a Radioprotector agent versus Placebo before External Beam Radiotherapy in Patients with Prostate Cancer to Reduce Radiation- induced Acute Bowel & Urinary Toxicity using RTOG Criteria

School of Paramedical Sciences, Shahid Beheshti Medical University,0 个研究点目标入组 36 人开始时间: 2012年1月20日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
36

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
o limit 至 o limit(—)
性别
Male

入选标准

  • Patients with Prostate Cancer Candidate for External Beam Radiotherapy

排除标准

  • Patients with Metastatic Prostate Cancer, Patients with Kidney & Liver dysfunction, Patients who receive any H2– Histamine receptor antagonist simultaneously, Patients with Allergic reaction in consequence of Famotidine Administration.

研究者

发起方
School of Paramedical Sciences, Shahid Beheshti Medical University,

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