IRCT20201227049851N1招募中3 期
Efficacy of Memantine augmentation in moderate to severe obsessive-compulsive symptoms
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 30
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
- •All patients who suffer from obsessive-compulsive disorder according to DSM V and clinical interview.
- •Patients who have Yale-Brown Scores of 15 and above.
- •Patients who give written consent for participating in the study.
排除标准
- •Patients who are diagnosed with a comorbid DSM V psychiatric diagnosis.
- •Patients who suffer from any systemic disease such as diabetes, hypo and hyperthyroidism,hypertension,hepatic failure or renal failure.
- •Patients who use alcohol or any other substance.
- •Patients who have received a psychotropic medicine during the last 6 months.
- •Women who are pregnant or breastfeeding or do not use any certain contraceptive method.
- •Patients who use concomitant somatic treatments.
- •Patients who are under treatment with Acetyl Cysteine, buprenorphine or any other medicine
- •Patients who receive any kind of psychotherapies.
研究者
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