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临床试验/CTRI/2024/11/076851
CTRI/2024/11/076851尚未招募4 期

Comparison of the effect of intrathecal fentanyl citrate and magnesium sulphate as adjuvants to hyperbaric levobupivacaine 0.5 per cent for spinal anaesthesia in patients undergoing lower limb orthopaedic surgeries A prospective randomised study

Gajra Raja Medical College and Jay Arogya Group of Hospitals1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年11月30日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
onset and duration of sensory and motor block, duration of analgesia

研究概览

简要总结

:

This prospective randomised study tocompare the effects of fentanyl vs magnesium sulphate as adjuvants to 0.5% hyperbaric levobupivacaine in orthopaedic surgeries under subarachnoid block shallinclude ninety ASA grade I and II patients aged 18-60 yrs undergoing orthopaedic surgeries. Group LS: 3ml 0.5% levobupivacaine heavy + 0.5ml normal saline. Group LF: 3ml 0.5% levobupivacaine heavy + fentanyl 25µg. Group LM: 3ml 0.5% levobupivacaine heavy + magnesium sulphate 50mg + 0.4ml normal saline. The onset and duration of sensory and motor block and intraoperative haemodynamics will be recorded. In the postoperative period, duration of analgesia, time to first request of analgesia, VAS scores, and side effects will be observed and compared amonf all three groups.

研究设计

研究类型
Interventional
分配方式
Other
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • •Patients consenting to participate in the study, aged between 18-60 years, of both sexes, of ASA grade I or II, admitted to undergo lower limb orthopaedic procedures in our institute were included in this study.

排除标准

  • •Patients declining consent, aged less than 18 or greater than 60 years, ASA grades III or IV, suffering from any respiratory, cardiac, hepatic, renal, neurological or coagulation disorder, pregnant or already receiving opioid or magnesium therapy or having any local infection at the site of injection of spinal anaesthesia were excluded from the study.

结局指标

主要结局

onset and duration of sensory and motor block, duration of analgesia

时间窗: onset of sensory and motor blockade at baseline | duration of sensory blockade when the spinal block regresses till S1 (in minutes) | duration of motor block till time of first mobilisation (in minutes) | duration of analgesia until the patient requests rescue analgesia at VAS score greater than 3

次要结局

  • haemodynamic parameters(baseline, intraoperative intervals predefined at 5, 10, 15, 30, 45, 60, 90, 120 & 150 minutes)
  • side effects(in the postoperative period)

研究者

发起方
Gajra Raja Medical College and Jay Arogya Group of Hospitals
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Anusha Tripathy

Gajra Raja Medical College

研究点 (1)

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