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Clinical Trials/NCT01004835
NCT01004835CompletedNot Applicable

The Migraine and Pain Study GeneBank at Scripps Clinic Registry (MAPS)

Scripps Translational Science Institute1 site in 1 country61 target enrollmentStarted: January 2009Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
61
Locations
1
Primary Endpoint
Gene identification

Study Overview

Brief Summary

The objective of this study is to obtain blood or saliva samples to define genes for migraine and pain diseases.

Detailed Description

It is estimated that over one-third of the world's population suffers from persistent or recurrent pain. Migraine is highly heritable and the majority of juveniles who suffer from the disorder have a mother or father who also have the disease. The blood or saliva samples will go through DNA analysis and be sequenced for candidate genes or subjected to whole-genome sequencing. By creating a MAPS GeneBank from these patients' blood/saliva donations we will ultimately be able to define genes for migraine and pain diseases.

Study Design

Study Type
Observational
Observational Model
Family Based

Eligibility Criteria

Ages
10 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Family members (genetic duo or trio), consisting of an adolescent 10 to 18 years of age and at least one of their biologic parents willing to be participate in trial
  • Adolescent and at least 1 biologic parent with Migraine diagnosis confirmed by Dr. Christy Jackson
  • Is reliable, cooperative and willing to comply with all protocol-specified procedures and/or sub-study if consented
  • Able to understand and grant informed consent

Exclusion Criteria

  • Patient has been previously enrolled in the MAP GeneBank at Scripps Clinic Registry
  • Has a significant chronic medical condition (i.e.chronic meningitis or a secondary origin/cause of headache) which, in the investigator's option, may interfere with the patient's optimal participation in the study
  • Treatment with any investigational agents or devices within 30 days preceding enrollment in the study
  • Has undergone ECT within 90 days preceding enrollment in the study

Outcomes

Primary Outcomes

Gene identification

Time Frame: end of study

By creating a MAPS GeneBank from these patients' blood/saliva donations we will ultimately be able to define genes for migraine and pain diseases.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Scripps Translational Science Institute
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Eric Topol, MD

Director, Scripps Translational Science Institute

Scripps Translational Science Institute

Study Sites (1)

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