跳至主要内容
临床试验/IRCT20170311033004N2
IRCT20170311033004N2尚未招募2 期

Evaluation of adjunctive therapy of propolis in the treatment of mild to moderate depression

Academic Center for Education, Culture and Research (ACECR)0 个研究点目标入组 68 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
68

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 65 years(—)
性别
All

入选标准

  • Individuals with diagnosis of mild-moderate depression according HDRS score
  • Age between 18-25
  • Patients with no comorbid disorders diabetes, high blood pressure or cardiovascular disease
  • Patients with no comorbid mental condition
  • No consumption drugs other than SSRI
  • Non-pregnant

排除标准

  • Diagnosis of another non-depression disorder for patient during study
  • Suicide inclination
  • Taking anti depression medication except SSRI or electroconvulsive therapy
  • impossibility to track disease (absence at the time of visit, cancellation of the continuation of the study and death)
  • Occurrence of allergic reaction
  • Occurrence of some side effect disorders such as fever, digestive and heart complications due to drug intake
  • Hospitalization

研究者

发起方
Academic Center for Education, Culture and Research (ACECR)

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Propolis effects on depressive disorder | 临床试验