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临床试验/CTRI/2018/01/011437
CTRI/2018/01/011437已完成未知

A comparative study of buprenorphine in twodifferent doses as an adjuvant to levobupivacaine inUSG guided unilateral lumbar plexus block forpostoperative analgesia after hip, thigh and kneesurgeries

Dr RPGMC Kangra at Tanda0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
90

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

  • 1. scheduled for hip, thigh and knee surgery under subarachnoid block.
  • 2. ASA class I-II.
  • 3. BMI 18.5-29.9.

排除标准

  • 1. Patientâ??s refusal either for spinal anesthesia or for lumbar plexus block.
  • 2. Patients with anatomical deformities.
  • 3. Patients having bleeding disorders.
  • 4. Patients with local infection at the sites where needle for spinal and lumbar plexus block is to be inserted.
  • 5. Patients having dysrhythmias on the ECG
  • 6. Patients allergic to study drugs.
  • 7. Patients who are opioid tolerant or opioid dependent.
  • 8. Patients on anticoagulants.
  • 9. Failure of spinal anesthesia.

研究者

发起方
Dr RPGMC Kangra at Tanda

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