An interventional study of Botulinum toxin and bupivacain in Vestibular Migraine, sponsored by Pamukkale University. Completed at 1 site in Turkey. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2025-06-04.
Sponsored by Pamukkale University · Not applicable, Interventional, and Treatment
There is no standard approach to the treatment of vestibular migraine. Agents used in the treatment of migraine are frequently used. In treating migraine, local anesthetic agents, nerve-blocking methods, and botulinum toxin local injection is commonly applied, and successful results are obtained. Adapting the nerve-blocking method used in the treatment of migraine to the treatment of vestibular migraine is the purpose of the study.
Patients between 18-75 diagnosed with/without aura or chronic migraine according to IHCD-3 diagnostic criteria and who describe dizziness during or between attacks will be evaluated in the ENT clinic.
Patients included in the study will be recorded as definite vestibular migraine or probable vestibular migraine according to criteria defined in the BARANY community and IHCD-3. Differential diagnosis of vertigo will be made with pure tone audiometry, Caloric test, VHIT, Videonystagmography, and cVEMP. MIDAS (migraine disability scale), DHI (dizziness handicap inventory), VSS (vertigo symptom scale), DASÖ-21 anxiety test, and Allodynia Symptom Checklist (ASKL) forms will be filled.
Patients will be randomly divided into two groups. Patients in the control group will be given beta-blocker therapy, the standard treatment. The local anesthetic agent bupivacaine will be injected into the greater/small occipital nerves and supratrochlear/ supraorbital nerves. Patients in the study group will be asked to keep a diary of pain, dizziness, and painkiller use for one month. At the end of the 1st month, the scoring will be repeated, and the patients who show a decrease in half will be accepted to the next stage, botulinum toxin application. BoNT/A botulinum toxin A (botox; Allergan) will be injected bilaterally into the same regionns. All scoring will be repeated in the 1st, 3rd and 6th months.
1,528 studies on the registry are indexed under Migraine Disorders; 299 are open to participants now.
This study's enrollment of 29 is below the median of 80 across 1,175 interventional studies indexed under Migraine Disorders.
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Exclusion Criteria:
patients who have vestibular migraine and who accepted for study gruoup as local anesthetic and botulinum toxin group
Procedure: Botulinum toxin and bupivacain
Botulinum toxin A AND bupivacain( local anesthetic)
MIDAS(Migraine Disability Assessment)
The MIDAS (Migraine Disability Assessment) questionnaire is used to measure the impact of headaches. It will be measured at baseline and 6 months after treatment to assess the effects of treatment on vestibular symptoms. Complete recovery will result in significant recovery (\>50%), moderate recovery (25-50% reduction), and minimal recovery (\<25%).
Time frame: 6 months
DHI(Dizziness Handicap Inventory)
The DHI is a 25-item self-report questionnaire that quantifies the impact of dizziness on daily life by measuring self-perceived handicap. It will be measured at baseline and 6 months after treatment to assess the effects of treatment on vestibular symptoms. Complete recovery will result in significant recovery (\>50%), moderate recovery (25-50% reduction), and minimal recovery (\<25%).
Time frame: 6 months
VSS(Vertigo symptom sclae)
The VSS assesses patient-reported symptoms of vestibüler disease. Complete recovery will result in significant recovery (\>50%), moderate recovery (25-50% reduction), and minimal recovery (\<25%).
Time frame: 6 months
The Depression, Anxiety and Stress Scale - 21 Items (DASS-21)
The relationship between the improvement of vertiginous symptoms and the improvement of psychiatric symptoms will be observed. To evaluate this result, the difference between baseline and post-treatment DASS-21 will be compared
Time frame: 6 months
Allodynia Symptom Checklist
The relationship between the improvement of vertiginous symptoms and cutaneous symptoms will be observed. To evaluate this result, the difference between baseline and post-treatment ASCL scores will be compared.
Time frame: 6 months
Plan to share: No
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This study is completed, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.
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Pamukkale University