IRCT20221015056178N1招募中3 期
76 patients who are candidates for surgery in hospitals affiliated with Islamic Azad University of Tehran are randomly divided into two groups. One hour before surgery, Mirtazapine will be given to the intervention group and placebo to the control group. After transferring the patients to the ward, the pain level of the patients is measured serially. We want to evaluate the preoperative effect of Mirtazapine administration on reducing postoperative pain (pain severity and duration of pain relief).
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 76
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
- 25 years 至 50 years（—）
- 性别
- All
入选标准
- •Patients who are candidates for surgery
- •Insensitivity to Mirtazapine
- •Age between 25 and 50 years
- •BMI between 20 and 25
- •ASA one or two
- •Patient consent to conduct a clinical trial
排除标准
- •Surgeries greater than an hour
- •Emergency surgeries
- •Pregnant women or the possibility of pregnancy
- •Diabetic, cardiac, pulmonary and neurological patients
- •Drug addiction
研究者
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