CTRI/2011/091/000101已完成4 期
TO STUDY THE ANALGESIC EFFICACY AND SAFETY PROFILE OF PARAVERTEBRAL BUPIVACAINE AS COMPARED TO INTRAVENOUS FENTANYL FOR ADULTS UNDERGOING PERCUTANEOUS NEPHROLITHOTOMY (PCNL) UNDER GENERAL ANAESTHESIA
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- one
- 入组人数
- 50
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
- •After obtaining institutional, ethics committee approval and informed written consent, the study will be conducted in 50, ASA Grade I and II, patients aged 18-65years undergoing percutaneous nephrolithotomy.
排除标准
- •1)Patients who refuse to participate in the study.
- •2)Patients with infection at the site of proposed block
- •3)Patients with severe chest wall deformity.
- •4)Patients having coagulopathy or receiving any anticoagulants.
- •5)Patients with known hypersensitivity to local anaesthetics.
- •6)Patients inability to understand the proper functioning and use of patient controlled analgesia (PCA) device due to any reason.
- •7)Patients who suffer from any intraoperative or postoperative complications like hydrothorax, urosepsis excessive bleeding, opposite side DJ stenting is done.
研究者
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