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Peripheral Nerve Block and Topiramate in the Treatment of Medication Overuse Headaches

CompletedNot applicableNCT03767062
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Purpose: In this study, the investigators compared the effectiveness of peripheral nerve block (greater occipital nerve block with supratrochlear nerve block) versus topiramate as detoxification therapies in chronic migraine patients with medication overuse headache. Methods: At least ninety chronic migraine patients with medication overuse headache are aimed to include in this study. Patients will be divided into the two groups. The first group will receive topiramate (n=45, estimated) and the second group will receive nerve block (n=45, estimated) as detoxification therapy. Patients' records regarding the visual analog scale (VAS) scores and headache frequencies are aimed to be collected before and after the therapy. Comparisons regarding VAS scores, headache frequencies, 50% responder rates and 75% responder rates will be performed in between topiramate and nerve block groups.

Study details

Official title
Comparison of Effects of Peripheral Nerve Block and Topiramate in the Treatment of Medication Overuse Headaches: A Randomised Parallel Group Study
Conditions
Interventions
  • Drug: Topamax
  • Procedure: Greater Occipital Nerve Block + Supratrochlear Nerve Block
Sponsor
Ataturk University
Start date
2019-03-01
Primary completion
2019-03-31
Sex
All
Age range
from 15 Years
Results posted
Yes, on ClinicalTrials.gov
Countries
Turkey (Türkiye)
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Chronic migraine diagnosis according to International Classification of Headache-2 Disorders (ICHD) 2. w/o pregnancy or breastfeeding. 3. w/o acute or chronic psychiatric disorders. 4. w/o nephrolithiasis. 5. w/o medication of anticoagulant and antiaggregant. 6. w/o allergy to topiramate or bupivacaine. 7. w/o prophylaxis within the last three months with any of; propranolol, nebivolol, topiramate, valproate, venlafaxine, duloxetine, amitriptyline, flunarizine. 8. w/o previous history of peripheral nerve block, botulinum toxin or acupuncture. 9. w/o history of multiple sclerosis, movement disorders, epilepsy, stroke, and tumor. J-w/o chronic systemic diseases including hypertension, cardiac insufficiency, diabetes, pulmonary disease, kidney disease, liver disease, and peripheral arterial disease. Exclusion Criteria: 1. Lost to follow up within the pretreatment period during the detoxification therapy after the detoxification therapy 2. could not tolerate the peripheral nerve block or topiramate

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03767062