Migraine?

  • STATUS
    Recruiting
Updated on 8 November 2020

Summary

Migraine?

Description

Have you suffered from at least 2 migraines per month for at least 3 months or more? Are you female, at least 18 years of age? Have you suffered from headaches during your last 2 or 3 menstrual cycles? If so, you may qualify to participate in a research study of an investigational drug to see if it can help prevent related migraines. For more information, please call: Diablo Clinical Research at 925-930-7267 Or visit our website at www.diabloclinical.com

Inclusion Criteria:

  • Patient who has had regular menstrual cycles monthly (22 to 32 days) for at least the last 3 cycles
  • Patient experiences headache during menstrual period in at least 2 out of last 3 cycles
  • Patient has history of migraine for = 3 months and with = 2 migraine attacks per month in the 2 months prior to screening
  • Patient agrees to use an effective method of birth control through the duration of the study

Exclusion Criteria:

  • Patient has basilar or hemiplegic migraine headache
  • Patient has taken medication for acute headache on more than 15 days per month in the 3 months prior to screening
  • Patient is taking prophylactic medication for migraine and daily dose has changed with in 4 weeks prior to screening
  • Patient has history of significant liver disease
  • Patient has had cardiac surgery or symptoms with in 3 months of screening
  • Patient has confounding pain syndromes, psychiatric conditions, dementia, or major neurological disorders other than migraine
  • Patient has history of neoplastic disease = 5 years prior to signing informed consent
  • Patient has history of gastric or small intestinal surgery
  • Patient consumes 3 or more alcoholic drinks per day

Details
Clinical Study IdentifierTX134954
Last Modified on8 November 2020

Eligibility

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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