CTRI/2022/01/039446尚未招募不适用
Comparison of Intravenous Tramadol vs Nalbuphine as analgesic in postoperative patients after General Anaesthesia
dr d y patil vidyapeeth pimpri pune1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年1月15日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- for analgesia
研究概览
简要总结
comparison of two drugs that is Tramadol and Nalbuphine for postoperative analgesia in patients undergoing procedures under general anesthesia. Will publish soon
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 21.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Adult patient between 18 years to 60 years of either sex
- •American Society of Anaesthesiologists (ASA) grade I &II undergoing elective surgeries under general anaesthesia • Weight of patient within normal range for that age andsex • Patients who are willing for the study and have given written informed consent.
排除标准
- •1.Patients with pre-existing cardiovascular diseases (IHD, hypertension, Valvular Heart diseases, deranged renal or liver functions.
- •2.Patients with physical dependence to opioids.
- •â€¢ Pregnant and lactating females.
- •â€¢ Patients with diabetes, asthma, epilepsy, bleeding disorder.
- •â€¢ Patients on monoamine oxidase, tricyclic antidepressants, selective serotonin reuptake inhibitors, andwarfarin • History of hypersensitivity to study drugs • Patients not willing to participate in the study will be excluded.
结局指标
主要结局
for analgesia
时间窗: 0, 2, 5, 15, 30 ,minutes
次要结局
- for analgesiA(for 30 mins to 2 hrs)
研究者
研究点 (1)
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