Efficacy of intranasal sphenopalatine ganglion block by lignocaine spray for the treatment of post dural puncture headache following spinal anaesthesia

INDIRA GANDHI INSTITUTE OF MEDICAL SCIENCES1 个研究点分布在 1 个国家目标入组 40 人开始时间: 2019年2月12日最近更新: 2022年1月13日

试验速览

阶段: 3 期
状态: 已完成
发起方: INDIRA GANDHI INSTITUTE OF MEDICAL SCIENCES
入组人数: 40
试验地点: 1
主要终点: efficacy of sphenopalatine ganglion block for the treatment of post dural puncture headache following spinal anaesthesia

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to evaluate two techniques for sphenopalatine ganglion block for post dural puncture headache. Lignocaine spray is a relatively non-invasive technique as compared to the standard technique.

研究设计

研究类型: Interventional
分配方式: Random Number Table
盲法: Participant and Outcome Assessor 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 assigned class 1 to 3, experiencing a post dural puncture headache within 7 days of dural puncture, patients giving consent to participate, vas score of pain 3 or more than 3, age 18 or more than 18 years.

排除标准

•allergy to study medication, <18 years og age, pain score on presentation <3/10 of headache, known nasal septal deviation or abnormalities such as polyp, patients with history of any disorder of nose such as sinusitis, rhinitis.

结局指标

主要结局

efficacy of sphenopalatine ganglion block for the treatment of post dural puncture headache following spinal anaesthesia

时间窗: Vas score will be assessed at 1/2hr,1hr,2hr,24hr,48hr,72hr and number of blocks required for relief

次要结局

adverse effect of sphenopalatine ganglion block, if any(upon discharge patients will be instructed for report when symptoms appear)

研究者

发起方

INDIRA GANDHI INSTITUTE OF MEDICAL SCIENCES

申办方类型

Government medical college

研究点 (1)

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