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临床试验/CTRI/2024/03/064131
CTRI/2024/03/064131尚未招募4 期

A comparative study of efficacy and safety of single drug 0.5% Ropivacaine on intraocular pressure before and after peribulbar block in cataract surgery with most commonly used mixture of 0.5% bupivacaine and 2% lidocaine with adrenaline : A randomised clinical trial - NI

BLDE0 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
4 期
状态
尚未招募
发起方
BLDE

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)Uncomplicated cataract.
  • 2)Normal intraocular pressure

排除标准

  • 1)Patients with cognitive impairment.
  • 2)Patients allergic to hyaluronidase, lidocaine, ropivacaine and bupivacaine.
  • 3)Any other surgeries combined with cataract.
  • 4)Patients with hypertension and coronary artery disease in lignocaine group.

研究者

发起方
BLDE

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