A Clinical Study Examining the Safety and Effectiveness of a New Medication (Keppra®) for the Prevention of Migraine Headaches

NCT ID: NCT00203216

Last Updated: 2011-08-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-09-30
• Study Completion Date: 2005-09-30

Brief Summary

The study drug levetiracetam is FDA approved as an add-on medication in the treatment of partial onset seizures in adults with epilepsy. The trade name is Keppra®. This is an "open-label" trial, which means that all participating patients will receive active study drug.

The Jefferson Headache Center has developed this clinical study to evaluate the safety and effectiveness of levetiracetam in preventing migraine headaches, with or without aura (visual disturbances).

In addition, the study site will be performing a procedure called Transcranial Magnetic Stimulation (TMS). This procedure measures brain activity because it is thought that people with migraine experience periods of cortical hyperexcitability or over-activity in the brain. This information may help physicians in the future determine which preventive medications will work for which patients.

Conditions

Migraine

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Levatiracetam

Subject titrated open-label study drug to maximally tolerated dose: maximum: 3000 mg. per date. (minimum allowed daily dose to remain in study: 1000)

Group Type: EXPERIMENTAL

levetiracetam

Intervention Type: DRUG

Daily dose of open label levatiracetam was 3000 mg. or maximally tolerated dose. (Maximum daily dose: 3000 mg. Minimum daily dose allowed for study participation:1000 mg)

Transcranial Magnetic Stimulation

Intervention Type: PROCEDURE

Interventions

levetiracetam

Daily dose of open label levatiracetam was 3000 mg. or maximally tolerated dose. (Maximum daily dose: 3000 mg. Minimum daily dose allowed for study participation:1000 mg)

Intervention Type: DRUG

Transcranial Magnetic Stimulation

Intervention Type: PROCEDURE

Other Intervention Names

Keppra

Eligibility Criteria

Inclusion Criteria

• Patient is male or female between the ages of 18 and 65
• Patient has an IHS diagnosis of migraine with or without aura for at least one-year prior to screening
• Patient has experienced between 4 and 10 migraine headaches per month over the past six months, with at least 48 hours separating attacks
• Patient is able to differentiate migraine attacks from other headache types, if applicable
• Patient is not currently and has not in the 4 weeks preceding screening received prophylactic treatment for the indication of migraine
• Patients daily medications have remained at a stable dose for the 4 weeks preceding screening
• Patient is using or agrees to use for the duration of participation a medically acceptable form of contraception (as determined by investigator), if female of child-bearing potential
• Patient has negative urine pregnancy test prior to study entry, if female of child-bearing potential
• Patient is able to understand and comply with all study requirements
• Patient provides written informed consent prior to any screening procedures being conducted

Exclusion Criteria

• Women who are pregnant or lactating
• Patients with onset of migraine after 50 years of age
• Patients who experience > 15 headache days per month
• Patients who have been previously treated or are currently being treated with levitiracetam
• Patients who have failed greater than 3 adequate trials of other antiepileptic drugs for the prevention of migraine.
• Patients who, in the investigators opinion, have a history or have evidence of a medical or psychiatric condition that would expose them to an increased risk of a significant adverse event or would interfere with the assessments of efficacy and tolerability during this trial
• Patients with an abnormal ECG that, in the investigators opinion, would expose them to increased risk of adverse events or interfere with study drug and/or analysis of efficacy/tolerability
• Patients who take medication for acute treatment greater than 10 days per month over the past three months.
• Patients who are allergic to or have shown hypersensitivity to compounds similar to levetiracetam
• Patients with a history of significant drug or alcohol abuse within the past year
• Patients who have had a suicidal ideation in the 3 months prior to screening or has a history of attempted suicide
• Patients who currently have or have a history of significantly impaired renal function
• Patients who have participated in an investigational drug trial in the 30 days prior to the screening visit
• Patients who have a Beck Depression Inventory score of > 18 at screening
• Patients who have > 0 on question number 9 of Beck Depression Inventory (Suicidal Thoughts or Wishes question)
• Patients who have a defibrillator or pacemaker, an implanted medication pump, a metal plate in the skull, or metal objects inside the eye or skull (e.g. a shrapnel wound).

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

UCB Pharma

INDUSTRY

Sponsor Role: collaborator

Thomas Jefferson University

OTHER

Sponsor Role: lead

Responsible Party

Thomas Jefferson University

Principal Investigators

William B Young, MD

Role: PRINCIPAL_INVESTIGATOR

Thomas Jefferson University, Jefferson Headache Center

Locations

Jefferson Headache Center

Philadelphia, Pennsylvania, United States

Countries

United States

Other Identifiers

080-19000-H80001

Identifier Type: -

Identifier Source: secondary_id

WBY/LEV01

Identifier Type: -

Identifier Source: org_study_id