Status:

RECRUITING

Enroll -HD: A Prospective Registry Study in a Global Huntington's Disease Cohort

Lead Sponsor:

CHDI Foundation, Inc.

Conditions:

Huntington's Disease

Eligibility:

All Genders

18+ years

Brief Summary

Enroll-HD is a longitudinal, observational, multinational study that integrates two former Huntington's disease (HD) registries-REGISTRY in Europe, and COHORT in North America and Australasia-while al...

Detailed Description

The primary objective of Enroll-HD is to develop a comprehensive repository of prospective and systematically collected clinical research data (demography, clinical features, family history, genetic c...

Eligibility Criteria

Inclusion

  • Carriers: This group comprises the primary study population and consists of individuals who carry the HD gene expansion mutation.
  • Controls: This group comprises the comparator study population and consists of individuals who do not carry the HD expansion mutation.
  • These two major categories can be further subdivided into six different subgroups of eligible individuals:
  • Manifest/Motor-manifest HD: Carriers with clinical features that are regarded in the opinion of the investigator as diagnostic of HD.
  • Pre-Manifest/-Motor-manifest HD: Carriers without clinical features regarded as diagnostic of HD.
  • Genotype Unknown: This group includes a first or second degree relative (i.e., related by blood to a carrier) who has not undergone predictive testing for HD and therefore has an undetermined carrier status.
  • Genotype Negative: This group includes a first or second degree relative (i.e., related by blood to a carrier) who has undergone predictive testing for HD and is known not to carry the HD expansion mutation.
  • Family Control: Family members or individuals not related by blood to carriers (e.g., spouses, partners, caregivers).
  • Community Controls: Individuals unrelated to HD carriers who did not grow up in a family affected by HD. Data collected from community controls will be used for generation of normative data for sub-studies.
  • Participant status will be captured in the study database using 2 variables: 1) Investigator Determined Status: this will be based on clinical signs and symptoms and genotyping performed as part of medical care, and will be updated at every visit; and 2) Research Genotyping Status: this will be based on genotyping conducted as part of Enroll-HD study procedures. Based on research genotyping, participants will be reclassified under this variable from Genotype Unknown to 'Carriers' or 'Controls'. Investigators and participants will be blinded to this reclassification.

Exclusion

  • Individuals who do not meet inclusion criteria,
  • Individuals with choreic movement disorders in the context of a negative test for the HD gene mutation.
  • For Community Controls: those individuals with a major central nervous system disorder will be excluded (e.g. stroke, Parkinson's disease, multiple sclerosis, etc.).
  • Participants under 18 may be eligible to participate (if they have juvenile-onset HD).

Key Trial Info

Start Date :

July 1 2012

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

January 1 2062

Estimated Enrollment :

35000 Patients enrolled

Trial Details

Trial ID

NCT01574053

Start Date

July 1 2012

End Date

January 1 2062

Last Update

February 28 2024

Active Locations (183)

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Page 1 of 46 (183 locations)

1

University of Alabama

Birmingham, Alabama, United States, 35294

2

St. Joseph's Hospital and Medical Center

Phoenix, Arizona, United States, 85013

3

University of California - Irvine Medical Center

Irvine, California, United States, 92697

4

Loma Linda Medical Center

Loma Linda, California, United States, 92354