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临床试验/CTRI/2023/02/049556
CTRI/2023/02/049556尚未招募不适用

Subarachnoid block for elective infraumbilical surgeries- Comparison of hyperbaric solutions of Levobupivacaine and Ropivacaine with Hyperbaric racemic bupivacaine- A randomised controlled trial

Dr Juliet Ann Abraham1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2023年10月2日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
105
试验地点
1
主要终点
Comparison of onset and duration of motor blockade

研究概览

简要总结

Spinal Anaesthesia is the gold standard for infraumbilical surgeries. Commonly used as spinal anaesthetic is 0.5% Hyperbaric Bupivacaine in spite of their cardiotoxic and neurotoxic property, if intravascular access is gained. This is due to the R- enantiomer component which has increased affinity for the sodium channels in cardiac tissue. This led to the formulation of levobupivacaine and ropivacaine, pure S-enantiomers and long acting local anaesthetic agents. Until recently Hyperbaric solutions of levobupivacaine and ropivacaine were not available. Hence this study. It is a proposed randomised control trial, where the patients are counselled regarding the procedure and their consent is attained. They are divided into groups of three with 35 in each given and given their allocated drug. The different parameters studied are the onset and duration of motor and sensory blockade, post-operative analgesia, hemodynamic parameters and complications. The results are then tallied to compare the efficiency and safety profile of levobupivacaine and ropivacaine against racemic bupivacaine.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
20.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • ASA I-11 Age 20- 70 years Height 150-180cms Infraumbilical surgeries >2 hours.

排除标准

  • Patient refusal Local infection Coagulopathies Allergy to the study drugs Any pre-existing neurological deficits Parturients.

结局指标

主要结局

Comparison of onset and duration of motor blockade

时间窗: The onset of the maximum motor blockade- attaining Grade 4 on the Modified Bromage scale- checked every 3 mins from the time of administration (3 mins, 6 mins, 9 mins, 12 mins) | The duration of the motor blockade- from the onset of the motor blockade [(Grade 4 on Modified Bromage scale), peaking at (Modified Bromage scale Grade 1)]till the effect of the drug is completely subsided (Modified Bromage scale Grade 6) - checked every 20 mins post-surgery (20 mins, 40 mins, 60 mins..120mins )

次要结局

  • 1. To compare the onset and duration of sensory blockade(The onset of the sensory blockade - blockade at the level of T10 dermatome - checked every minute from the time of administration of the drug (1 min, 2 min, 3 min, 4 min, 5 min))
  • To compare the total consumption of rescue analgesia when the comparator agent and interventional agents are administered(The total consumption of rescue analgesia is determined by the need for intravenous analgesics for the first 6 hours post-surgery (1st hour, 2nd hr...6th hour))
  • Comparison of intraoperative hemodynamic profile and occurrence of adverse effects with each study drug(Vitals are recorded every two minutes from the time of administration of the drug (0 min, 2 mins, 4 mins...) for the first 20 minutes and then every 5 minutes till the end of the surgical procedure.)

研究者

发起方
Dr Juliet Ann Abraham
申办方类型
Other [self]

研究点 (1)

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