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临床试验/CTRI/2024/12/078110
CTRI/2024/12/078110尚未招募不适用

Comparative Study Between Nalbuphine V/S Magnesium Sulphate As An Adjuvant To Intrathecal Hyperbaric Levobupivacaine In Infraumbilical Abdominal Surgeries

Hind Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2024年12月24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
80
试验地点
1
主要终点
Comparison of block characteristics in terms of Time taken for onset of sensory and motor blocks. Duration of sensory and motor blocks

研究概览

简要总结

TITLE- COMPARATIVE STUDY BETWEEN NALBUPHINE V/S MAGNESIUM SULPHATE AS AN ADJUVANT TO INTRATHECAL HYPERBARIC LEVOBUPIVACAINE IN INFRAUMBILICAL ABDOMINAL SURGERIES

Introduction - Regional anaesthesia (RA) significantly reduces pre- and postoperative side effects and is preferred over general anaesthesia due to fewer complications, early onset, and specific action. Spinal anaesthesia, widely used for infraumbilical surgeries, offers reversible sensory, motor, and sympathetic blockade with minimal systemic effects, utilizing hyperbaric, isobaric, or hypobaric solutions. Levobupivacaine, a safer S(-) enantiomer of bupivacaine, has lower cardiotoxicity and neurotoxicity, acting through sodium channel blockade. Nalbuphine, a semisynthetic opioid with μ antagonist and Κ agonist effects, enhances analgesia with minimal side effects when used intrathecally. Magnesium, via NMDA receptor antagonism, supports pain modulation but has limited CSF penetration.

Hypothesis -

Null Hypothesis:

Adjuvant use of Nalbuphine is equal in every aspect to MgSO4

for comparison when given with levobupivacaine.

Alternate Hypothesis:

Adjuvant use of Nalbuphine provides better block characteristics as

compared to MgSO4.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant 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

  • ASA-1 and ASA-2 Age 18yrs to 60 yrs.

排除标准

  • Patient Refusal Pregnancy Obesity Contra Indication to Spinal Anaesthesia Allergy to Study Drug Patients with Cardiac, Liver and Renal Disease Previous Surgery of Lumbar Spine.

结局指标

主要结局

Comparison of block characteristics in terms of Time taken for onset of sensory and motor blocks. Duration of sensory and motor blocks

时间窗: Assess the heart rate, blood pressure, oxygen saturation and MAP

次要结局

  • Duration of analgesic effect, Peak VAS pain scores during recovery period, Total amount of rescue analgesia used. Post-operative hemodynamic changes.(Assess the VAS Score , Vitals in Post-operative period every 30 mins till 2 hours and every 1 hour till 12 hours, time taken for first rescue Analgesia.)

研究者

发起方
Hind Institute of Medical Sciences
申办方类型
Other [none]
责任方
Principal Investigator
主要研究者

Dr Samundra Saini

Hind Institute of Medical Sciences

研究点 (1)

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