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临床试验/CTRI/2024/12/078608
CTRI/2024/12/078608尚未招募4 期

Comparison of ultrasound guided anterior quadratus lumborum block versus combined pericapsular nerve group block with lateral femoral cutaneous nerve block in hip surgeries-Prospective randomised control trail

Sri Ramachandra Institute of Higher Education and Research1 个研究点 分布在 1 个国家目标入组 60 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
入组人数
60
试验地点
1
主要终点
Amount of rescue analgesia consumption

研究概览

简要总结

Patient who fit in to inclusion criteria will be enrolled into the study after getting written informed consent from the patient. All patient’s assessment will be done on the previous day and nil per oral orders will be given as per department protocol.Baseline blood pressure and heart rate will be recorded before shifting to operating room.After shifting to operating room electrocardiography, non invasive blood pressure and oxygen saturation will be connected. A total of 60 patients of ASA I and II(aged 20-60 years) undergoing hip surgeries will be randomly allocated into two groups of 30 each.Group 1 will receive ultrasound guided anterior quadratus lumborum block with 25 ml of 0.25% ropivacaine with 0.1mg/kg of dexamethasone and Group 2 will receive combined pericapsular nerve group block (22ml) with lateral femoral cutaneous nerve block (3ml) with 0.25% ropivacaine with 0.1 mg/kg of dexamethasone before spinal anesthesia.Intraoperatively  heart rate, non invasive blood pressure and oxygen saturation will be monitored every 3 minutes for first 15 minutes and at 5 minutes for next 15 minutes.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • American Society of Anesthesiologist (ASA) I and II.

排除标准

  • Patient refusal for participation Known coagulation disorder Allergies to study drugs Chronic pain Morbidly obese Emergency surgeries.

结局指标

主要结局

Amount of rescue analgesia consumption

时间窗: 0 hour,2 hours,4 hours,8 hours,12 hours,24 hours

次要结局

  • Post operative pain intensity(NRS scale)(Duration of analgesia)

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

DR Mohammed Arfak H

Sri Ramachandra Institute of higher education and research

研究点 (1)

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