NCT00051324Active, not recruiting
Neurobiological Predictors of Huntington's Disease (PREDICT-HD)
Neurobiological Predictors of Huntington's Disease Trial
Source: ClinicalTrials.gov · Last updated 14 Jan 2025
Brief summary (registry, in English)
The purpose of this trial is to study early brain and behavioral changes in people who have the gene expansion for Huntington's disease, but are currently healthy and have no symptoms.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 1700 (estimated)
- First submitted
- 8 Jan 2003
- Start date
- Aug 2002
- Primary completion date
- 30 Jun 2025
- Lead sponsor
- Jordan Schultz
- Diseases
- Huntington's disease
- NCT number
- NCT00051324
What you commit to
- Study type: Observational
- Planned participants: 1700
- From Aug 2002 to the primary completion date, 30 Jun 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- current treatment with antipsychotic medications, including the traditional neuroleptics such as haloperidol as well as the atypical antipsychotics risperidone, clozapine, quetiapine, and olanzapine;
- treatment with phenothiazine-derivative antiemetic medications such as prochlorperazine, metoclopramide, promethazine, and Inapsine on a regular basis (greater than 3 times per month);
- Specific exclusion criteria for the lumbar puncture:
Other illness
- clinical evidence of unstable medical or psychiatric illness (including substance abuse);
- history of sever learning disability or mental retardation;
- history of other CNS disease or event (e.g., seizures or head trauma);
Lab values
- Current use of anti-platelets
Other
- diagnosis of manifest HD (at least 50% confidence by neurologist that symptoms are present);
- Current use of anti-coagulants
- Unable to provide consent for him/herself
Who the study is looking for
- men and women at risk for HD, who have been tested for the HD gene mutation, and who have not been diagnosed with symptoms of HD (CAG ≥36 for CAG-expanded group or CAG \<36 for CAG-norm group).
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Iowa Coordinator of this site? Confirm its status | Iowa City | United States | Unknown status |
Related publications
- Discovery and Targeted Proteomic Studies Reveal Striatal Markers Validated for Huntington's Disease.Ann Clin Transl Neurol · 2026 · PMID 41363816
This page is information, not medical advice. Discuss any trial with your doctor.