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临床试验/NCT07512219
NCT07512219尚未招募不适用

Comparative Study of Greater Occipital Nerve Block and Pulsed Radiofrequency in the Management of Chronic Migraine : Clinical Outcomes and Neurophysiological Correlates A Prospective Randomized Study

Sohag University0 个研究点目标入组 70 人开始时间: 2026年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
70
主要终点
The change in the VAS score of Pain over period of follow up

研究概览

简要总结

Comparative Study of Greater Occipital Nerve Block and Pulsed Radiofrequency in the Management of Chronic Migraine : Clinical Outcomes and Neurophysiological Correlates A Prospective Randomized Study

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patient with Diagnosis of chronic migraine for > 3 months.
  • migraine days ≥ 15 days/month.
  • Failure or inadequate response to standard medical treatment.

排除标准

  • Secondary headache disorders.
  • Coagulopathy or anticoagulant therapy.
  • Infection at injection site.
  • History of cervical spine surgery.
  • Pregnancy or breastfeeding.
  • Previous PRF or occipital nerve surgery within last 3 months

研究组 & 干预措施

Group of Greater Occiptal nerve Block , GONB

Active Comparator

Injection Procedure:

  1. Local skin infiltration with 1-2 mL of 1% lidocaine at puncture site.
  2. GON block using 3-5 mL of local anesthetic, optionally combined with 20-40 mg triamcinolone ( Bilaterally )
  3. Needle placement confirmed by ultrasound visualization of the nerve and spread of injectate.
  4. Observe patient for 15-20 minutes post-injection for immediate adverse events.

干预措施: Greater occiptal nerve block (Drug)

Group of Pulsed Radiofrequency , PRF

Active Comparator
  1. Introduce RF cannula adjacent to GON under ultrasound guidance.
  2. Confirm sensory stimulation: paresthesia at occipital scalp at <0.5 V.
  3. PRF settings:
  • Temperature: ≤42°C
  • Pulse duration: 20 ms
  • Frequency: 2 Hz
  • Duration: 120 seconds per cycle, 2 cycles per side
  1. Continuous monitoring of patient comfort and vital signs.

干预措施: Pulsed radiofrequency (Device)

结局指标

主要结局

The change in the VAS score of Pain over period of follow up

时间窗: 6 months

after do GONB and Pulsed radio frequency we assess improvement of Episodic Pain over period of Follow up

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Shehab Mahmoud Mohamed

assistant lecturer in faculty of medicine sohag university

Sohag University

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