CTRI/2021/03/031875已完成未知
EFFICACY OF DULOXETINE IN PATIENTS WITH CENTRAL POST-STROKE PAIN: A RANDOMISED DOUBLE BLIND PLACEBO CONTROLLED STUDY
INSTITUE OF MEDICAL SCIENCES BH0 个研究点目标入组 82 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 82
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
入选标准
- •Ã¢â?¬Â¢Aged 18 years or older
- •Ã¢â?¬Â¢Positive history of hemorrhagic or ischemic stroke with lesion in the unilateral brain region proved by computed tomography or magnetic resonance imaging of the brain
- •Ã¢â?¬Â¢Presence of signs and symptoms in accordance with a decrease in pain and heat sensations in the affected part of the body
- •Ã¢â?¬Â¢Presence of spontaneous or stimulated pain in the affected side, which could be smaller or the same in size as the sensory impairment area, fulfilling the mandatory criteria proposed by Klit et al.
- •Ã¢â?¬Â¢Patients with moderate to severe pain (Numeric Rating Scale (NRS) score of 4 and higher) are included.
- •Ã¢â?¬Â¢ Patients who are already on any other drugs for CPSP can be included in the study after providing a washout period of two weeks
- •Ã¢â?¬Â¢Only first episode stroke patients to be taken in the study.
排除标准
- •Ã¢â?¬Â¢Not willing to participate in the study
- •Ã¢â?¬Â¢Lack of imaging findings compatible with stroke (like tumors)
- •Ã¢â?¬Â¢Likely peripheral causes of pain (pain due to spasticity, nociceptive, psychogenic causes)
- •Ã¢â?¬Â¢Hypersensitivity to duloxetine
- •Ã¢â?¬Â¢Previous treatment with SNRIs
- •Ã¢â?¬Â¢Pregnant or lactating women
研究者
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