跳至主要内容
临床试验/CTRI/2013/02/003395
CTRI/2013/02/003395招募中3 期

Randomized controlled single blind trial to compare efficacy and safety between Diclofenac Sodium and Tramadol in post LSCS analgesia in patients of Preeclampsia. - Nil

Dr Borade Sanjio Bhimraoji0 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
招募中
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

  • Post LSCS patients with PE from PNC ward of Gynecology and Obstetrics Deptt ready to give informed consent.

排除标准

  • 1.Patient with Eclampsia.
  • 2.Patient with PE with Renal Failure.
  • 3.Patient with PE with Cardiac decompensation.
  • 4.Normotensive patients who underwent LSCS for other obstetric indications other than PE.

研究者

发起方
Dr Borade Sanjio Bhimraoji

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