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临床试验/CTRI/2024/12/078735
CTRI/2024/12/078735尚未招募4 期

A study to compare the efficacy of dexmedetomidine and fentanyl as adjuvants to ropivacaine in USG guided axillary block for upper limb surgeries

Dipti1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2025年1月10日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
36
试验地点
1
主要终点
To compare the onset and duration of sensory and motor blockade of dexmedetomidine versus fentanyl as an adjuvant to ropivacaine in axillary block in patients undergoing forearm surgeries

研究概览

简要总结

It is a prospective , randomised , double blinded comparative study to compare the efficacy of dexmedetomidine and fentanyl as an adjuvants in axillary block in patients undergoing upper limb surgeries

Parameters that will be compared between the two groups will be the onset and duration of action of sensory and motor blockade, duration of analgesia and side effects

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator 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 2 patients -Patients posted for upper limb surgeries -Written consent from the concerned patients.

排除标准

  • ASA3 or more -Below 18 years and above 60 years -Patients with major neurological, cardiac, respiratory, metabolic and coagulation abnormalities -Patients contraindicated for regional technique -Patient with known allergies to local anaesthetics.

结局指标

主要结局

To compare the onset and duration of sensory and motor blockade of dexmedetomidine versus fentanyl as an adjuvant to ropivacaine in axillary block in patients undergoing forearm surgeries

时间窗: After administering the block, comparison between the two groups of onset and duration of sensory and motor blockade, duration of analgesia will be assessed at baseline, after injection of study drug at 5 mins, 10 mins, 30 mins and 10 mins after surgery

次要结局

  • Compare the duration of postoperative analgesia & observe the side effects of dexmedetomidine & fentanyl as an adjuvant to ropivacaine in axillary block in patients undergoing forearm surgeries(Duration of analgesia will be assessed post surgery once the effects of the block decrease & time of rescue to analgesia will be assessed 2 hours after surgery & hourly until intervention is required)

研究者

发起方
Dipti
申办方类型
Other [[self]]
责任方
Principal Investigator
主要研究者

Dipti

Dr.D.Y.Patil Medical College, Hospital and Research Centre

研究点 (1)

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