CTRI/2024/06/068402尚未招募4 期
Comparative evaluation of different doses of intrathecal morphine in reducing the requirement of postoperative epidural analgesia in patients undergoing major abdominal surgery: A randomized controlled trial - NI
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
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
- •Patients 18 years or older, both male and female, American Society of Anaesthesiology (ASA) grade I and II, undergoing major abdominal surgery will be considered for this study.
排除标准
- •Patients who refuse to consent for the study.
- •Patients with ASA grade III or higher.
- •Patients in sepsis or septic shock.
- •Patients with respiratory diseases like chronic obstructive pulmonary disease, asthma, restrictive lung disease etc. or cardiac diseases like ischemic heart disease, arrythmias etc.
- •Patients with spine deformities.
- •Patients with liver disease or coagulopathy.
- •Opioid dependent patients.
- •Those with a history of chronic pain syndromes or chronic opioid use (more than 60 mg oral morphine equivalent daily).
- •Any patient requiring post-operative ventilatory support in view of surgical reasons, hemodynamic instability, acid base imbalance or hypothermia.
研究者
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