跳至主要内容
临床试验/CTRI/2018/01/011593
CTRI/2018/01/011593尚未招募4 期

Comparision of three doses of heavy Bupivacaine in spinal anaesthesia in patients undergoing lower extremity surgery.

Ramapati Sanyal1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2018年1月31日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Change in pulse systolic diastolic and mean blood pressure

研究概览

简要总结

Spinal anaesthesia is  the anaesthesia of choice in adults undergoing lower limb surgery,provided there is no significant co-morbidity. But spinal anaesthesia can cause hypotension , bradycardia and prolonged immobilisation which can be harmful and distressing to the patient. The aim of the present study was to compare three different doses of bupivacaine  for lower limb surgery in sixty ASA grade 1 and 2 patients aged 18 to 80 yrs of age. The parameters used will be systolic, diastolic and mean blood pressure and pulse rate. The secondary parameters will be recession of sensory and motor block at 2 hours using two dermatomal recession and modified bromage scale.

研究设计

研究类型
Interventional
分配方式
Random Number Table
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • ASA 1 and 2 Undergoing lower limb surgery.

排除标准

  • Patient refusal.
  • Anatomically distorted spine.
  • Spine surgery.
  • Surgery extending beyond 3 hrs.
  • Patients with perioperative complications.

结局指标

主要结局

Change in pulse systolic diastolic and mean blood pressure

时间窗: 2 hours

Time to first analgesic requirement.

时间窗: 2 hours

次要结局

  • Recession of sensory and motor block using two segment recession time and modified Bromage scale respectively.(4 hours)

研究者

发起方
Ramapati Sanyal
申办方类型
Other [self]

研究点 (1)

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