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临床试验/CTRI/2013/10/004075
CTRI/2013/10/004075已完成4 期

ReSOnS trial- REctus Sheath block for postoperative analgesia in gynaeco-ONco Surgical patients â?? a double blinded randomized controlled trial. - ReSOnS trial

Tata Memorial Hospital0 个研究点目标入组 74 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
入组人数
74

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

  • Women 18- 75 years of age with ASA 1& 2 who are listed for elective midline abdominal surgery for the treatment of primary gynaecological cancer

排除标准

  • 1.1.Refusal to consent
  • 2.Emergency surgery
  • 3.Conversion following Laparoscopic surgery
  • 4.Palliative surgery
  • 5.Surgery for recurrent disease
  • 6.History of previous laparotomy
  • 7.Surgery in view of suspected intra abdominal infection
  • 8.History of hepatic, renal disease or cardio-pulmonary disease- in cases in which diclofenac or paracetomol is contraindicated
  • 9.Patient with platelet count less than 50,000 or Patient with deranged coagulopathy INR. 1.5
  • 10. Obesity , BMI more than 35
  • 11.Weight less than 50 kg

研究者

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