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临床试验/CTRI/2025/11/098221
CTRI/2025/11/098221尚未招募4 期

Comparison of ultrasound guided lesser occipital & greater auricular nerve block (LOGAB) versus superficial cervical plexus block for postoperative analgesia in adults undergoing elective mastoid surgery under general anaesthesia: A randomized controlled trial

Self1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2025年12月10日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
Self
入组人数
75
试验地点
1

研究概览

简要总结

Mastoid surgeries are now commonly performed for middle ear pathologies. They are

usually associated with moderate degree of post operative pain. Various modalities like

intravenous NSAIDs, opioids and regional nerve blocks are used to attenuate the

degree of post operative pain.(1) In regional anaesthesia techniques, superficial cervical plexus block, greater auricular nerve block, auriculotemporal nerve block are often used for pain relief

Study Design:

A randomized prospective, placebo-controlled trial

Study Duration: 1 year

Participants will be randomized into 3 groups using a computer-generated table.

Concealment of allocation will be done with sealed, numbered, opaque, white

envelopes which will be opened after the patient is taken into the OR.

Group I (n=25): will receive ultrasound guided LOGAB (lesser occipital greater auricular

block) with 5 ml of 0.25% Ropivacaine

Group II (n=25): will receive ultrasound guided superficial cervical plexus block with 10

ml of 0.25% Ropivacaine.

Group III (n=25): will receive conventional opioid analgesia only.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patients scheduled for elective mastoid surgery 2.ASA I-II patients.

排除标准

  • Presence of local infection or impaired skin integrity at the injection site
  • Any cognitive or psychiatric condition that prevents comprehension and completing the outcome measures
  • Patients receiving anticoagulant therapy
  • Pregnancy or breastfeeding
  • Previous neck surgery or radiation.

研究者

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

Dr Ravneet Kaur Gill

Dr B R Ambedkar State Institute of Medical Sciences

研究点 (1)

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