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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
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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Iowa
Coordinator of this site? Confirm its status
Iowa CityUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.