Status:

RECRUITING

Characterization of Patients With Uncommon Presentations and/or Uncommon Diseases Associated With the Cardiovascular System

Lead Sponsor:

National Heart, Lung, and Blood Institute (NHLBI)

Conditions:

Metabolic Disease

Obesity

Eligibility:

All Genders

1-100 years

Brief Summary

Background: \- Researchers are interested in studying individuals who have known or suspected metabolic, inflammatory or genetic diseases that may put them at a high risk for heart diseases or diseas...

Detailed Description

We propose to characterize the etiology and natural history of rare and uncommon diseases, both known and unknown that present with symptoms and signs associated with the risk of overt or potential ca...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Eligible subjects may include anyone over 1 year of age who is affected with diseases/disorders (index cases), or who is a relative of a person who is affected with diseases/disorders. Relatives may include genetic carriers and non-carriers.
  • Healthy adult volunteers must be 18 years of age or older, and must agree to have blood or tissue samples studied, and potentially stored for future research.
  • Index cases enrolled in this protocol will have been referred with a known or suspected pathology that may be associated with cardiovascular dysfunction or risk with a suspected atypical presentation, heritable disorder, or genetic predisposition. The investigator with expertise in the presentation of the subject, along with consulting specialists, will review the medical history and may review any medical records that are available of prospective subjects and offer admission based upon the potential to help the individual, to learn from the subject, or to initiate clinical or basic research suggested by the subject s workup.
  • EXCLUSION CRITERIA:
  • Persons of less than 1 year of age or greater than 100 years of age
  • Healthy volunteers unable to give informed consent or who decline to have blood and/or tissue studies, or who do not consent to have samples stored for future research may be excluded from this study.
  • Pregnant women
  • Persons who are not fluent in the English language will be excluded from Patient Reported Outcome Questionnaires. Such persons would be unable to properly complete questionnaires that are only valid in the English language.

Exclusion

    Key Trial Info

    Start Date :

    July 21 2010

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    Estimated Enrollment :

    5000 Patients enrolled

    Trial Details

    Trial ID

    NCT01143454

    Start Date

    July 21 2010

    Last Update

    December 31 2025

    Active Locations (2)

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    Page 1 of 1 (2 locations)

    1

    Suburban Hospital

    Bethesda, Maryland, United States, 20814

    2

    National Institutes of Health Clinical Center

    Bethesda, Maryland, United States, 20892