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Clinical Trials/NCT01517425
NCT01517425
Enrolling By Invitation
Not Applicable

Evaluating Cardiovascular Phenotypes Using Induced Pluripotent Stem Cells

Scripps Translational Science Institute1 site in 1 country200 target enrollmentNovember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Artery Disease
Sponsor
Scripps Translational Science Institute
Enrollment
200
Locations
1
Primary Endpoint
iPSC development
Status
Enrolling By Invitation
Last Updated
last year

Overview

Brief Summary

This research is being done to understand how changes in DNA may put people at risk for developing coronary artery disease. Stem cells will be made using cells from blood and/or skin biopsy samples. We are trying to understand which specific changes in DNA negatively impact a person's health.

Registry
clinicaltrials.gov
Start Date
November 2012
End Date
July 2030
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Scripps Translational Science Institute
Responsible Party
Principal Investigator
Principal Investigator

Eric Topol, MD

Director, Scripps Translational Science Institute

Scripps Translational Science Institute

Eligibility Criteria

Inclusion Criteria

  • Previously enrolled in the CAD module of the Genebank at Scripps Clinic Registry
  • Eligible to have their blood drawn
  • Be reliable, cooperative and willing to comply with all protocol-specified procedures
  • Able to understand and grant informed consent
  • Previously enrolled in the Healthy Elderly Active Longevity (HEAL) Cohort
  • Eligible to have their blood drawn
  • Be reliable, cooperative and willing to comply with all protocol-specified procedures
  • Able to understand and grant informed consent

Exclusion Criteria

  • Unwilling or unable to grant informed consent.
  • Have a significant medical condition that in the Investigator's opinion may interfere with subject's study participation.

Outcomes

Primary Outcomes

iPSC development

Time Frame: five years

Develop methods of iPSC generation from patients with genomic risk.

Study Sites (1)

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