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临床试验/CTRI/2020/05/025249
CTRI/2020/05/025249尚未招募不适用

"Comparison of two different doses of Dexmedetomidine combined with 0.5 % Levobupivacaine for post operative analgesia in ultrasound guided supraclavicular brachial plexus block-A double blinded randomized cantrolled study"

CHETTINAD HOSPITAL AND REASERCH INSTITUTE1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2020年5月20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
56
试验地点
1
主要终点
every 30 min till the onset of pain

研究概览

简要总结

Patients who are posted for elective and emergency upperlimb procedures

Patients who are classified under american society of anaesthesiologists,who comes under ASA-1 and ASA-2

For elective surgeries adequate NPO status of six hours is maintained preoperatively

T.Dizepam 5mg and T.Rantac150 mg is given preoperative night before surgery

For emergency procedure NPO status of six hours is followed

A total number of 56 patients are allocated randomly using computer generated code,Group 50 receives 29 ml of 0.5% levobupivacaine groupD75 recieves 75 microgram of dexmedatomidine and 29 ml of 0.5 percent levobupivacaine

Motor onset and sensory onset are recorded

Surgeries done only under block

Intraoperative and post operative hemodynamic variables are recorded for each patient

Patient shifted to surgical ICU after the procedure and post operatively patient is monitored

If patient have VAS score more than 3/10 then rescue analgesia is given with tramadol 100 mg

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
17.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • All ASA-1 AND ASA-2 patients undergoing either elective or emergency upperlimb surgical procedure.

排除标准

  • Pediatric patients Geriatric patients(age more than 70 years) Patients with known comorbities(diabetes,hypertension,asthma,seizure disorder,hypothyroidism) patients who are allergic to local anaesthetic drugs Patients who are not not willing for surgical procedure under regional anaesthesia.

结局指标

主要结局

every 30 min till the onset of pain

时间窗: every 30 min after injecting drug till the onset of pain

次要结局

  • effect on hemodynamics(onset and duration of of sensory and motor blokade)

研究者

发起方
CHETTINAD HOSPITAL AND REASERCH INSTITUTE
申办方类型
Research institution and hospital

研究点 (1)

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