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临床试验/CTRI/2021/03/031678
CTRI/2021/03/031678尚未招募未知

RANDOMISED CLINICAL TRIAL OF SUBCUTANEOUS VERSUS INTERFASCIAL BUPIVACAINE VERSUS NO LOCAL ANAESTHETIC FOR PAIN CONTROL AFTER MIDLINE LAPAROTOMY - RSF

St Johns Medical College 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

  • Patients aged 18 or above who is undergoing abdominal surgery both elective and emergency through a midline laparotomy incision of length 15-25cm

排除标准

  • Patients undergoing midline laparotomy due to trauma.
  • Patients who had peritonitis.
  • History of hypersensitivity or adverse reaction to the medications being used.
  • Patients with chronic liver or renal disease
  • History of previous midline laparotomy
  • Body mass index greater than 30kg/m2
  • Those patients who did not give consent for study.

研究者

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