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Track-HD

Track-HD - Track-HD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON31178
Enrollment
90
Registered
2007-09-18
Start date
2008-03-23
Completion date
Unknown
Last updated
2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Huntington's disease

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Ability to tolerate MRI and sample donation;• Subjects will be either: 1. Control subject a. Partner/spouse of a patient, not at risk of HD b. Known non-carriers for HD (after genetic testing);2. Premanifest gene carrier a. Positive genetic test with CAG repeat length >= 40 and b. Burden of pathology score [(CAG-35.5) × age] >250 and c. Absence of diagnostic motor features according to the UHDRS 99;3. Early HD a. Positive genetic test with CAG repeat length >= 40 and b. Presence of diagnostic motor features according to the UHDRS 99 and c. Shoulson and Fahn stage 1 (TFC > 9-13) or 2 (TFC >= 7) according to the UHDRS 99 - functional capacity

Exclusion criteria

Exclusion criteria: • Stage 3 (TFC

Design outcomes

Primary

MeasureTime frame
All variables are considered to be primary study parameters: clinical, MRI, genetics and biomarkers to determine which combination is the most sensitive to detect changes in the natural course of HD.

Secondary

MeasureTime frame
Dependant on results on the primary outcome variables.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)