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Search / Trial NCT00915473

Greater Occipital Nerve Block for Migraine Prophylaxis

Launched by MAYO CLINIC · Jun 5, 2009

Trial Information

Current as of May 19, 2025

Completed

Keywords

ClinConnect Summary

Migraine is a common disease with lifetime prevalence in women and men of 33% and 12% respectively. Chronic migraine affects 2% of the US population and is highly disabling. There are no FDA approved medications for the treatment of chronic migraine.

Although some patients benefit from a daily prophylactic medication, others continue to suffer from severe, frequent, debilitating headaches. Limited efficacy, poor compliance, side effects and drug-drug interactions may explain why more than 80% of migraineurs in the population are not prescribed daily prophylactic medications.

Occipital ner...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Subjects meet diagnostic criteria for episodic migraine or chronic migraine according to the International Headache Classification II (ICHD-II)
  • Migraine sufferers who experience at least 1 attack per week
  • Able to read and understand the requirements of the study, abide by any restrictions, and return for the required examinations
  • Able and willing to sign an informed consent statement
  • Subjects must be in generally good health as confirmed by medical history, medication review, baseline physical examination, vital signs and clinical laboratory evaluations.
  • Exclusion Criteria:
  • Subjects with continuous headache (no headache free periods)
  • Subjects using maintenance opioid medication
  • Subjects who have started a medication with prophylactic migraine efficacy within the past 2 months
  • Known hypersensitivity or allergic reaction to any of study ingredients (lidocaine, bupivicaine, any local anesthetics, and corticosteroids) or betadine.
  • Use of any investigational medication within 90 days of the initial screening visit and/or concurrent enrolment in an investigational study
  • Injection site infection or systemic infection at the injection visit (afebrile at time of injection)
  • Presence of cranial bone defect
  • Subjects with chronic cluster headache, new daily persistent headache, hemicrania continua, or chronic tension type headache
  • Subjects with a history of an unstable medical condition (e.g. cardiovascular, hepatic, renal, endocrine) that may impair their reliable participation in the study or necessitate the use of medications not permitted in this study
  • Subjects with a history (within the past 6 months) of a major psychiatric disorder that in the opinion of the investigator may preclude the subject from completed the requirements of the study
  • Female subjects who are pregnant or nursing
  • Subjects with a history of drug or alcohol abuse within the past 2 years
  • Subjects with a history of poor compliance with past drug therapies, as judged by the investigator.

About Mayo Clinic

Mayo Clinic is a renowned nonprofit medical practice and research institution dedicated to providing comprehensive healthcare and advancing medical knowledge through innovative research and education. With a commitment to patient-centered care, Mayo Clinic conducts numerous clinical trials aimed at exploring new therapies and improving treatment outcomes across various disciplines. Leveraging a multidisciplinary approach, the institution collaborates with leading experts and cutting-edge technology to ensure rigorous scientific standards and ethical practices in all its research endeavors. Through its trials, Mayo Clinic seeks to translate breakthroughs in science into tangible benefits for patients, fostering advancements in medicine that enhance health and quality of life.

Locations

Phoenix, Arizona, United States

Patients applied

0 patients applied

Trial Officials

David W. Dodick, M.D.

Principal Investigator

Mayo Clinic

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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