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临床试验/IRCT20211022052836N1
IRCT20211022052836N1已完成早期 1 期

Evaluation of the effectiveness of adding sarcosine to PMT (parental education management) treatment on the symptoms of coping disorder

Esfahan University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
80

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
6 years 至 12 years(—)
性别
All

入选标准

  • 1. Girl and boy children aged 6 to 12 years who have been diagnosed with coping disorder by a psychiatrist based on the DSM-V. 2. Parents' consent to participate in the study

排除标准

  • 1- Patients who do not want to continue participating in the study at any stage. 2- Patients who do not plan their medication according to the prescribed medication and do not take it accurately. 3- Patients for whom another diagnosis is made during the study.

研究者

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