Volunteers needed for a Migraine medical research study

Updated on 23 November 2020


Volunteers needed for a Migraine medical research study


You may qualify for a research study which evaluates the effectiveness and safety of an investigational medication given by injection in individuals who suffer from moderate to severe headaches and migraines. Volunteers will receive 3 doses of the study medication or placebo. This study will access the change in migraine frequency, intensity and duration. If you currently take a medication to prevent migraines you will be allowed to continue your current treatment. Eligible volunteers can expect 5 visits over 4 months.

Monetary compensation is available for time and travel expenses. No insurance is required. If you, your family members, friends or co-workers are interested in volunteering for this migraine research study please contact us at 856-3784 or text STUDY to 72727 on Smartphone (standard text rates apply) or submit interest at www.coastalcarolinaresearch.com .

Please note that all persons who respond to the study via the internet are asking us to contact them regarding the study by telephone, also your names and contact information may be entered into our patient database when we speak with you and only with your permission. All information provided by the subject during the course of this study will be treated as confidential.

All research study-related care is provided to qualified participants at no cost including:

  • Investigational medication or placebo
  • Physical exams
  • Lab tests including pregnancy test (for females)
  • ECG

Condition Migraine and Cluster Headaches
Clinical Study IdentifierTX138846
Last Modified on23 November 2020


Yes No Not Sure

Inclusion Criteria

To qualify participants must
Be 18 to 65 years of age
Suffer from moderate to severe headaches and migraines
Be in general good health
Females must have a reliable method of birth control
Clear my responses

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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