跳至主要内容
临床试验/CTRI/2020/08/027221
CTRI/2020/08/027221尚未招募未知

Comparison of sensory blockade and duration of post operative analgesic effect between bupivacaine heavy and bupivacaine heavy plus tramadol intrathecally in patients undergoing gynecological surgeries.

Shree krishna hospital0 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
未知
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

  • ASA grade 1-3 physical status

排除标准

  • Hypersensitivity to local anesthetics, absolute contraindications to spinal anesthesia that is patients refusal, any bleeding diathesis patients, local site infection,relative contraindications like severe hypotension, obstructive cardiomyopathies, any spinal deformity, spinal cord injnury

研究者

相似试验