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Recruiting Observational

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

NCT01574053 · tracked via the Priya Life Science Italy tracker
Sponsor
CHDI Foundation, Inc
Phase
Observational
Started
2012-07
Last updated
2024-02-28

Condition(s) studied

Huntington's Disease

Study 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 also expanding to include sites in Latin America. More than 30,000 participants have now enrolled into the study. With annual assessments and no end date, Enroll-HD has built a large and rich database of longitudinal clinical data and biospecimens that form the basis for studies developing tools and biomarkers for progression and prognosis, identifying clinically-relevant phenotypic characteristics, and establishing clearly defined endpoints for interventional studies. Periodic cuts of the database are now available to any interested researcher to use in their research - visit www.enroll-hd.org/for-researchers/access-data/ to learn more.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * 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 Criteria: * 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).

Primary outcome measure(s)

  • Motor Assessments: Unified Huntington's Disease Rating Scale (UHDRS) 99 Motor, UHDRS '99 Diagnostic Confidence Level — through study completion, an average of 1 year
    The motor section of the UHDRS assesses motor features of HD with standardized ratings of oculomotor function, dysarthria, chorea, dystonia, gait, and postural stability. UHDRS 99 Motor, UHDRS Diagnostic Confidence Level.
  • Functional Assessments: UHDRS '99 Total Functional Capacity, UHDRS '99 Functional Assessment Scale, UHDRS '99 Independence Scale — through study completion, an average of 1 year
    The Total Functional Capacity, Functional Assessment and Independence Subscales of the UHDRS '99 will be used to assess participants' functional status. The Total Functional Capacity scale has established psychometric properties including inter-rater reliability and validity, based on radiographic measures of disease progression.
  • Problem Behaviors Assessment-Short (PBA-s) — through study completion, an average of 1 year
    The Problem Behavioral Assessment Short Version (PBA-s) will be used to perform behavioral assessments. This instrument measures frequency and severity of symptoms related to altered affect, thought content and coping styles.
  • Cognitive Assessments: Symbol Digit Modality Test; Stroop Color Naming; Stroop Word Reading; Categorical Verbal Fluency — through study completion, an average of 1 year
    Cognition will be assessed using the Categorical Verbal Fluency Test, Symbol Digit Modality Test and Stroop Color and Word Reading Test. Verbal fluency is a commonly used neuropsychological test which examines the ability to spontaneously produce words orally within a fixed time span. For category fluency, words must be produced according to semantic constraints. The measure of performance used will be the number of correctly generated words within 60 seconds.

Trial sites (183)

FacilityCityRegionStatus
University of Alabama Birmingham Alabama Recruiting
St. Joseph's Hospital and Medical Center Phoenix Arizona Recruiting
University of California - Irvine Medical Center Irvine California Recruiting
Loma Linda Medical Center Loma Linda California Terminated
University of California - Los Angeles Los Angeles California Recruiting
University of California - Davis Sacramento California Recruiting
University of California - San Diego San Diego California Recruiting
University of California - San Francisco San Francisco California Recruiting
Cenexel Rocky Mountain Clinical Research, LLC Englewood Colorado Recruiting
University of Connecticut Farmington Connecticut Recruiting
Georgetown University Washington D.C. District of Columbia Recruiting
University of Florida Board of Trustees Gainesville Florida Recruiting
University of Miami Miami Florida Recruiting
University of South Florida, HDSA Center of Excellence at USF Tampa Florida Recruiting
Emory University, Wesley Woods Health Center Atlanta Georgia Recruiting
Georgia Health Sciences University Augusta Georgia Terminated
Northwestern University Chicago Illinois Recruiting
University of Chicago Chicago Illinois Terminated
Rush University Medical Center Chicago Illinois Recruiting
University of Illinois College of Medicine at Rockford Rockford Illinois Terminated
Indiana University Indianapolis Indiana Recruiting
University of Iowa Iowa City Iowa Recruiting
University of Kansas Medical Center Kansas City Kansas Recruiting
Hereditary Neurological Disease Center Wichita Kansas Recruiting
University of Louisville Louisville Kentucky Recruiting
University of Maryland School of Medicine Baltimore Maryland Withdrawn
Johns Hopkins University Baltimore Maryland Recruiting
Boston University Medical Center Boston Massachusetts Terminated
Beth Israel Deaconess Medical Center Boston Massachusetts Recruiting
University of Michigan Ann Arbor Michigan Recruiting
Wayne State University Detroit Michigan Withdrawn
Hennepin County Medical Center Minneapolis Minnesota Recruiting
Washington University in St. Louis St Louis Missouri Recruiting
University of Nebraska Medical Center Omaha Nebraska Recruiting
Cleveland Clinic - Las Vegas Las Vegas Nevada Recruiting
Cooper University Hospital Camden New Jersey Active Not Recruiting
Rutgers, the State University of New Jersey New Brunswick New Jersey Recruiting
Albany Medical College Albany New York Recruiting
Columbia University New York New York Recruiting
University of Rochester Rochester New York Recruiting

+ 143 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01574053 on ClinicalTrials.gov ↗ ← All trials in Italy