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Clinical Trials/NCT03712917
NCT03712917
Completed
Not Applicable

Comparison of Therapeutic Effects of Greater Occipital Nerve Block, Topiramate, and Flunarizine on Episodic Migraine: A Randomised Parallel Group Study

Ataturk University1 site in 1 country120 target enrollmentMarch 1, 2019

Overview

Phase
Not Applicable
Intervention
Greater Occipital Nerve Block
Conditions
Migraine
Sponsor
Ataturk University
Enrollment
120
Locations
1
Primary Endpoint
Attack Frequencies
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Background: Preventive drug therapy in migraine aims to reduce the attack frequency, severity and duration of headache. Flunarizine and topiramate are widely used in the prevention of migraine attacks. Greater occipital nerve block (GONB) is an alternative treatment option for the prophylactic treatment of migraine. In this study, investigators compared the effectiveness of GONB, topiramate, and flunarizine in terms of reduction in post-treatment VAS scores and attack frequencies in patients with episodic migraine in a four-week period.

Material and Methods: At least one hundred and twenty migraine patients are aimed to be randomly divided into three treatment groups, namely flunarizine (n=40, estimated), topiramate (n=40, estimated) and GONB (n=40, estimated). The patients will be followed up for four weeks and the attack frequencies and VAS scores will be recorded weekly. At the end of the fourth week, the response rates based on 50% and 75% or more reduction in the VAS scores and attack frequencies will be calculated. Group-wise comparisons will be assessed statistically.

Registry
clinicaltrials.gov
Start Date
March 1, 2019
End Date
March 31, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mustafa Ceylan

Principal İnvastigator

Ataturk University

Eligibility Criteria

Inclusion Criteria

  • Migraine diagnosis according to ICHD-2
  • Ages between 15 -45 Volunteering
  • Monthly attack number between 5-14
  • BMI between 18-30
  • w/o history of nephrolithiasis
  • w/o history of DM, peripheral vascular disease
  • w/o history of chronic systemic diseases (lung, heart,liver, kidney)
  • w/o any detected CNS disease (including MS, movement disorders, CVD, primary or secondary tumors)
  • w/o history of acute or chronic psychiatric disease
  • w/o history of antiplatelet and anticoagulant medication

Exclusion Criteria

  • Lost to follow up
  • exited with his/her own will
  • detected primary headache during follow up
  • cessation due to adverse effects of topiramate
  • cessation due to adverse effects of flunarizine

Arms & Interventions

Greater Occipital Nerve Block

The GONB solution is prepared with 1 ml triamcinolone (40mg), 2 ml bupivacaine (10 mg), and 1 ml 0,9% NaCl. The solution is administered using a 22G × 1¼" (0.7 × 40mm) injector with the patient lying prone on the table. Injection is applied to medial of the occipital artery localized at the medial one-third of the superior nuchal line between the occipital tubercle and mastoid process. The scalp is cleaned with iodine before the procedure, and the injections are performed bilaterally at a volume of 2 mL after negative aspiration for blood.

Intervention: Greater Occipital Nerve Block

Topiramate

Topiramate is administered twice a day at a dose of 25 mg/day, which is increased to 100 mg/day in the second week.

Intervention: Topiramate

Flunarizine

Flunarizine is introduced with a single dose of 10 mg/day.

Intervention: Flunarizine

Outcomes

Primary Outcomes

Attack Frequencies

Time Frame: Post treatment 4 weeks

Number of headaches patients suffer in a month.

Visual Analog Scale

Time Frame: Post treatment 4 weeks

Range Pain 0-10, 0: No pain, 10: Worst Pain

Study Sites (1)

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