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临床试验/CTRI/2017/08/009249
CTRI/2017/08/009249尚未招募4 期

â??Clinical evaluation of efficacy and safety of transversus abdominis plane block inj. Bupivacaine vs. inj. Ropivacaine for post operative analgesia following lower segment cesarean section: a prospective, randomized, controlled, double blind study.â??

Department of Anaesthesiology0 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

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

  • ï??Informed written consent for
  • participation in study.
  • ï??Age: 20-35 years
  • ï??Gender: Antenatal female patients
  • scheduled for elective or non urgent
  • lower segment cesarean section.
  • ï??ASA physical status I and II.
  • ï??Patients refusing consent.

排除标准

  • 1.Contraindications to Spinal Anaesthesia like,
  • Local infection or sepsis at the site of
  • Lumbar puncture
  • Bleeding disorders, thrombocytopenia
  • Space occupying lesions of the brain
  • Anatomical disorders of the spine
  • Hypovolaemia e.g. following massive
  • haemorrhage
  • 2.Allergy to local anaesthetic drugs and NSAIDS.
  • 3.Patient on any form of analgesics therapy.
  • 4.BMI >= 25 kg/m2

研究者

发起方
Department of Anaesthesiology

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