Transcutaneous Supraorbital Nerve Stimulator Versus Topiramate in Prevention of Recurrent Migraine

Last updated: August 23, 2022
Sponsor: Tongji Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

Migraine (Adult)

Migraine (Pediatric)

Oral Facial Pain

Treatment

N/A

Clinical Study ID

NCT05516251
2021-S203
  • Ages 18-60
  • All Genders

Study Summary

Migraine has been ranked as the second most disabling neurological disorder in the worldwide. Medication or nonpharmacological treatments are all reasonable options for the prevention. Oral topiramate treatment is a typical effective method, while transcutaneous supraorbital nerve stimulation (SNS) was reported to be valuable for migraine acute treatment and even the prevention. As a new nonpharmacological therapeutic method, whether SNS is equivalent to topiramate is still unknown. The aim of the present study was to compare their effects in a cohort of migraine patients. After diagnosed with recurrent or chronic migraine and consented to this research, patients received randomly treatments by either SNS or topiramate, and were followed up prospectively. After a 1-month period of baseline observation, patients were followed by a 1-month treatment, and next 2-month period of followup. At least the following assessments will be performed: (1) Change from baseline in the number of migraine days during the 3 observing months; (2) Change from baseline in the number of moderate/ severe headache days over the 3 observing months; (3) 50% responder rate for the reduction of migraine days (percentage of patients having at least 50% reduction of migraine days) during the first treating month. Comparison of outcome measures between the 2 treatment groups will be performed to show the equivalence of SNS versus topiramate.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Aged 18-60 years old;
  • Diagnosed with definite migraine (ICHD-3 code 1.1 or 1.2);
  • At least 2 migraine attacks per month during the past 3 months;
  • Consent to participate in the study;
  • No contraindications to associated treatments.

Exclusion

Exclusion Criteria:

  • Received preventive treatments during the previous 3 months;
  • Definite other kinds of headache, especially tension-type, medication overuse andsecondary headache (ICHD-3 code 8.2);
  • Severe neurological or psychiatric disorders;
  • Severe primary systemic disorders including heart, brain, liver, kidney, andhematopoietic system;
  • Women with pregnancy or lactation.

Study Design

Total Participants: 200
Study Start date:
October 01, 2021
Estimated Completion Date:
September 30, 2023

Connect with a study center

  • Wensheng Qu

    Wuhan, Hubei 430030
    China

    Active - Recruiting

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