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临床试验/CTRI/2020/07/026304
CTRI/2020/07/026304尚未招募不适用

Comparison of the maximum sensory level achieved in Subarachnoid block between hyperbaric Bupivacaine and hyperbaric Bupivacaine along with Fentanyl: A Randomized Control Trial

Jawaharlal Institute of Postgraduate Medical Medical Education and Research1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2020年8月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
200
试验地点
1
主要终点
To compare the maximum sensory level achieved in Subarachnoid block with bupivacaine and bupivacaine along with fentanyl.

研究概览

简要总结

Subarachnoid block is the commonly practiced anaesthesia for surgeries of lower abdominal and lower limb. It enables the patient to be fully awake and avoids the side effects of anaesthetic drugs and gases. Intrathecal bupivacaine is most commonly preferred local anaesthetics these days to attain the surgical plane of anaesthesia/adequate sensory and motor blockade. Fentanyl is lipophilic opioid administered intrathecally as adjuvants to bupivacaine. It helps in increasing the duration of anaesthesia, depth of sensory blockade and reducing the dosage of local anaesthetics.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

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 undergoing elective surgeries under subarachnoid block with American Society of Anaesthesiologists (ASA) Physical status I and II.

排除标准

  • i.Allergy to drugs being used ii.Patient with neuromuscular diseases iii.Pregnant women iv.Symptomatic bradycardia v.Any contraindication for Subarachnoid block.

结局指标

主要结局

To compare the maximum sensory level achieved in Subarachnoid block with bupivacaine and bupivacaine along with fentanyl.

时间窗: After 20 minutes of the procedure i.e subarachnoid block

次要结局

  • To identify the association of the maximum sensory level achieved in Subarachnoid block with various physical parameters of patients (weight, height, body mass index, abdominal girth and vertebral column length) undergoing lower abdominal and lower limb surgeries.(just before performing the procedure)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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