跳至主要内容
临床试验/NL-OMON31671
NL-OMON31671已完成3 期

Double-blind placebo-controlled randomized study to determine the effectiveness of magnesium oxide to reduce the prostate motion. - Magnesium oxide to reduce prostate motion.

niversitair Medisch Centrum Utrecht0 个研究点目标入组 92 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
92

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 99(—)

入选标准

  • Prostate cancer patients scheduled for external beam radiotherapy using fiducial marker-based position verification.

排除标准

  • -Patients with known severe constipation
  • -Patients who receive laxatives
  • -Patients with a history of abdominal surgery
  • -Patients with known abdominal diseases (M. Crohn, colitis ulcerosa, diverticulitis )
  • -Patients with known severe renal failure or creatinine clearance of < 50 ml/min/1.73 m2
  • -Patients who receive tetracyclines, digoxine, iron or ciprofloxacine and the intake of this medication must be at the same time as the study medication
  • -Patients with known kidney stones
  • -Patients with known heart block

研究者

发起方
niversitair Medisch Centrum Utrecht

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