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临床试验/CTRI/2024/06/068402
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

ALL INDIA INSTITUTE OF MEDICAL SCIENCES RISHIKESH0 个研究点目标入组 0 人开始时间: 待定最近更新:

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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