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临床试验/CTRI/2023/04/052061
CTRI/2023/04/052061尚未招募不适用

A comparative study between Pericapsular nerve group block and femoral nerve blockusing ropivacaine 0.2% 25ml for ease of positioning to central neuraxial block in HIPsurgeries

ESIC Medical college and hospital1 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2023年1月5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
78
试验地点
1
主要终点
1.Efficacy of PENG block

研究概览

简要总结

PURPOSE : A comparative study between Pericapsular nerve group block and Femoral nerve block using 25ml of 0.2% Ropivacaine for ease of positioning to central neuraxial block for Hip surgeries.

DESIGN : RANDOMIZED,CONTROLLED TRAIL

PARTICIPANT AND CONTROL : Patients undergoing Hip surgeries will be Randomly allocated to one of the two groups based on computer generated random number.

INTERVENTION : Site of injection is marked, under strict aseptic precautions and USG guided 25ml Local anaesthetic agent is administered after negative aspiration.

Inj. Ropivacaine 0.2% 25ml is administered in incremental dose after negative aspiration for every 5ml using 22G Spinal needle or 10cm stimiplex block needle.

Group P will receive 25mls of 0.2% Ropivacaine for pericapsular nerve group block

Group F will receive 25mll of 0.2% Ropivacaine for femoral nerve block

Vitals and VAS score is monitored from time of injection till position for central neuraxial block.

Pain Score and Angle of sitting position to administer central neuraxial block is noted.

MAIN OUTCOME MEASURES : Efficacy of Pericapsular nerve group block for positioning of patient for central neuraxial block

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
50.00 Year(s) 至 90.00 Year(s)(—)
性别
Male

入选标准

  • Patients of either sex, 2) 50–90 years of age, 3) American Society of Anesthesiologists (ASA) physical grading I–III were included in the study.

排除标准

  • Exclusion criteria included patient refusal to participate in the study, 2) Presence of any coagulation disorders, 3) Presence of multiple fractures, 4) Any patients with head injury or other injuries,.

结局指标

主要结局

1.Efficacy of PENG block

时间窗: 40mins

2.Ease of positioning for central neuraxial block

时间窗: 40mins

次要结局

  • not applicable(not applicable)

研究者

发起方
ESIC Medical college and hospital
申办方类型
Government medical college

研究点 (1)

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