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临床试验/CTRI/2025/07/091316
CTRI/2025/07/091316尚未招募4 期

Comparison between the efficacy of dexmedetomidine versus magnesium sulphate as adjuvants to 0.5 percent ropivacaine in axillary brachial plexus block in hand and forearm surgeries

Pratikshya Nath1 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2025年8月1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
81
试验地点
1
主要终点
To compare the efficacy of dexmedetomidine versus magnesium sulphate as adjuvants to 0.5% ropivacaine in axillary brachial plexus block in hand and forearm surgeries

研究概览

简要总结

It is a prospective , randomized, double blinded comparative study to camparethe efficacy of dexmedetomidine versus magnesium sulphate as adjuvants to 0.5% ropivacaine in axillary brachial plexus block in hand and forearm surgeries.

The parameters  that need to be studied are the onset and duration of motor and sensory blockade and the time at which rescue analgesia is required.

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 grade I and II patients Aged between 18-60 years of either sex.
  • Patients undergoing hand and forearm surgery.
  • Availability of informed consent.

排除标准

  • Patients with ASA physical status III or more.
  • Patients with below 18 years and above 60 years.
  • Patients posted for emergency procedures.
  • Patients with major neurological, cardiac, respiratory, metabolic, renal, hepatic disease or with coagulation abnormalities.
  • Patients with known allergies to the local anaesthetics.

结局指标

主要结局

To compare the efficacy of dexmedetomidine versus magnesium sulphate as adjuvants to 0.5% ropivacaine in axillary brachial plexus block in hand and forearm surgeries

时间窗: The effects of the block needs to be assessed at baseline, after drug administration, after 5,10,15,30,45,60,90,120,150,180 minutes and at the end of surgery

次要结局

  • To compare the efficacy of dexmedetomidine versus magnesium sulphate as adjuvants to 0.5% ropivacaine in axillary brachial plexus block in hand & forearm surgeries on the basis of duration of block, bromage scale, VAS score & requirement of any postop analgesia(To assess the duration of analgesia post surgery with the help of VAS score system every 2 hourly till 24 hours post surgery)

研究者

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

Pratikshya Nath

Dr D.Y. Patil Medical college and hospital and Research center

研究点 (1)

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