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Neuroimaging biomarkers in Huntington*s Disease after more than 16 years of disease progression

Neuroimaging biomarkers in Huntington*s Disease after more than 16 years of disease progression - HD16MR: Neuroimaging biomarkers in HD 16 years later.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON57274
Enrollment
48
Registered
2024-02-12
Start date
2025-05-14
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Huntington's Disease Huntington's Disease

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Individuals with an age of 21 years or above, whom have participated in TRACK-HD at the Leiden-site, with the ability to give informed consent and undergo MRI scanning.

Exclusion criteria

Exclusion criteria: • Inability to understand the information about the protocol; • Severe chorea that, in the investigator*s judgment, precludes the patient*s participation in and completion of the MRI. • Contra-indication to MRI scanning, such as: - Claustrophobia; - Pregnancy; - Pacemakers and defibrillators; - Nerve stimulators; - Intracranial clips; - Intraorbital or intraocular metallic fragments; - Cochlear implants; - Ferromagnetic implants; - Hydrocephalus pump; - Intra-utrine device (not all types); - Permanent make-up (not all); - Tattoos above the shoulders (not all).

Design outcomes

Primary

MeasureTime frame
The main study parameters are the neuroimaging markers, starting with the primary outcome measurement: 1. Atrophy of subcortical regions such as caudate nucleus and putamen, and cortex 2. Measures of iron accumulation in the basal ganglia and cortex 3. Levels of metabolites, especially neuroinflammation metabolites, in the putamen. We will compare these measures with the previous MRI outcome measurements from TRACK-HD.

Secondary

MeasureTime frame
The secondary parameters are the clinical outcome measures, derived from the clinical assessments during this study, during TRACK-HD and the years in between during the Enroll-HD study. In addition, Q-motor assessments will be conducted and compared to available TRACK-HD measurements to evaluate longitudinal changes in objective motor function. 

Countries

Netherlands

Contacts

Public ContactS.C.M. Brama

Leids Universitair Medisch Centrum

s.c.m.brama@lumc.nl071-526 801

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jun 11, 2026