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临床试验/CTRI/2015/06/005869
CTRI/2015/06/005869已完成2 期

Comparison of caudal morphine with bupivacaine or bupivacaine alone for post operative analgesia in patients with ankylosing spondylitis undergoing total hip replacement surgery under general anaesthesia.

SUMIT BANSA0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
30

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

  • i)Age > 18 and < 60 years.
  • ii)ASA grade I & II patients.
  • iii)Patients diagnosed to ankylosing spondylitis.
  • iv)Patients scheduled for total hip replacement surgery

排除标准

  • 1.ASA grade III / IV
  • 2.History of bleeding /coagulation disorders.
  • 3.Prolonged prothrombin time ( > 3 secs. as compared to control) or low platelet count ( < 1,00,000 / mm3 ).
  • 4. Revision THR surgery.
  • 5.Pregnant patients
  • 6.Morbid obesity ( BMI >= 40 kg/m2 ).
  • 7.History of focal neurological deficit.
  • 8.Congenital abnormality of sacrococcygeal area.
  • 9.History of sensory or motor disorders of limb to be operated.
  • 10.Patients with active infection at site of caudal block.
  • 11.History of allergy to local anaesthetics.
  • 12. History of regular opioid use.
  • 13. Inability to comprehend VAS assessment scale.
  • 14. Inability to understand the use of patient controlled analgesia (PCA) device

研究者

发起方
SUMIT BANSA

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