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临床试验/CTRI/2025/12/099641
CTRI/2025/12/099641尚未招募不适用

Comparison of dexmedetomidine and fentanyl as an adjuvent to 0.5 % isobaric levobupivacaine in thoracic segmental spinal anaesthesia for patients undergoing Percutaeneous Nephrolithotomy.

Dr Swapnali Sarjerao Suryawanshi1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年12月31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
50
试验地点
1
主要终点
To compare the effect of addition of two adjuvent drugs Dexmedetomidine and Fentanyl in Isobaric Levobupivacaine in thoracic segmental spinal anaesthesia in patients undergoing Percutaeneous Nephrolithotomy on haemodynamic parameters, onset and duration of motor and sensory block, duration of analgesia and perioperative complications

研究概览

简要总结

This is an observational cross sectional study comparing the effect of addition of two adjuvant drugs Dexmedetomidine and Fentanyl in Isobaric Levobupivacaine in thoracic segmental spinal anaesthesia in patients undergoing Percutaeneous Nephrolithotomy on following parameters

1)Haemodynamics

2)Onset of motor and sensory block

3)Duration of motor and sensory block

4)Duration of analgesia

  1. Perioperative complications

Study is to be conducted on 50 patients divided into 2 groups of 25 each.

研究设计

研究类型
Observational

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 willing to sign informed consent for undergoing elective thoracic segmental spinal anaesthesia 2)Patients above 18 years and below 60 years of age 3)Patients belonging to American Society of Anaesthesiologists physical status I, II and III.

排除标准

  • Patients contraindicated for spinal anaesthesia 2)Patients with known allergy, sensitivity or any other form of reaction to the study drug 3)Pregnant or lactating patients or patients presenting for emergency surgeries.

结局指标

主要结局

To compare the effect of addition of two adjuvent drugs Dexmedetomidine and Fentanyl in Isobaric Levobupivacaine in thoracic segmental spinal anaesthesia in patients undergoing Percutaeneous Nephrolithotomy on haemodynamic parameters, onset and duration of motor and sensory block, duration of analgesia and perioperative complications

时间窗: To note the effect every 5 minutes for first 15 minutes then every 30 minutes till the end of surgery for next 5 hours

次要结局

未报告次要终点

研究者

发起方
Dr Swapnali Sarjerao Suryawanshi
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Swapnali Sarjerao Suryawanshi

Parul Institute of Medical Sciences and Research

研究点 (1)

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