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临床试验/CTRI/2013/02/003344
CTRI/2013/02/003344已完成4 期

Intrathecal Ropivacaine versus Intrathecal Ropivacaine and Tramadol for Lower Limb Orthopaedic Surgeries

CMS and GTB Hospital0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
60

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

  • Male patients with femur fractures, who belong to ASA class I or II and are between 18-60 years of age will be recruited for the study.

排除标准

  • Patients with a known hypersensitivity to any of the drugs, bilateral lower limb fractures, contraindications to regional anaesthesia, gross spinal deformity, emergency surgery and peripheral neuropathy will be excluded from the study. Patients with height less than 150 cm or more than 180 cm will also be excluded.

研究者

发起方
CMS and GTB Hospital

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