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临床试验/IRCT2016110120071N3
IRCT2016110120071N3已完成未知

Evaluation the efficacy of Achillea wilhelmsii capsule in irritable bowel syndrome patients:a randomized double blind placebo controlled clinical trial

Vice – Chancellery of Research, Kermanshah University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
90

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 years 至 60 years(—)
性别
All

入选标准

  • Inclusion criteria : age>18 ; ability to swallow the capsule ; patients who sign the testimonials and cooperate during the study ; patients who are not cured with Achillea wilhelmsii during a last month ; Patients who their diseases are approved by complete medical evaluation.
  • Exclusion criteria : pregnant patients and nursing mothers ; patients with any active stomach-interic disease ; patients who have to use other drugs that interference with this medication (such as laxative? antidepressants? opioid and narcotic analgesics ) ; patients who are disposed to a serious health danger, such as severe cardiac, liver or renal diseases ; If significant side effects occur, the patient will be excluded from the study ; patients with severe allergy to this plant (dermatitis contact) will be excluded.

排除标准

  • 未提供

研究者

发起方
Vice – Chancellery of Research, Kermanshah University of Medical Sciences

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