跳至主要内容
临床试验/CTRI/2009/091/000736
CTRI/2009/091/000736已完成3 期

Intrathecal levobupivacaine 0.5% versus Intrathecal bupivacaine 0.5% for spinal anesthesia.

aprod Lifesciences Pvt Ltd.Reg Office 304, Town Centre, Andheri-Kurla Road, Andheri, Mumbai- 4000590 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
200

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. ASA Grade I and II. 2. Weight - 50 to 80 kg.
  • 3. Height - 140 to 180 cm.
  • 4. Age - 18 to 60 yrs.
  • 5. Surgeries on the lower limbs, pelvis and lower abdomen.

排除标准

  • 1.Patient?s refusal to participate in the study.
  • 2.ASA Grade III, IV and V.
  • 3.Age below 18 years and above 60 years.
  • 4.Weight below 30 kg and above 80 kg.
  • 5.Patients with history of allergy to any drug.

研究者

发起方
aprod Lifesciences Pvt Ltd.Reg Office 304, Town Centre, Andheri-Kurla Road, Andheri, Mumbai- 400059

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