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临床试验/IRCT20181009041286N1
IRCT20181009041286N1已完成3 期

Comparison of response to two regimens of Lactolose and Bisacodyl in the treatment of acute constipation in patients with acute stroke

Kashan University of Medical Sciences0 个研究点目标入组 50 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
入组人数
50

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
no limit 至 no limit(—)
性别
All

入选标准

  • Admission within 48 hours of onset of symptoms
  • Definite stroke diagnosis and confirmation with CT-Scan or MRI
  • Acute constipation

排除标准

  • Patients with constipation before stroke
  • History of colon or rectum cancer
  • Constipation caused by metabolic disorder such as hypokalemia
  • Taking drugs that cause constipation, such as anticholinergic drugs or drugs with anticholinergic effects, calcium blockers, etc.
  • History of diabetes mellitus
  • History of myocardial infarction
  • History of hypothyroidism

研究者

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