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NCT00018889 · ClinicalTrials.gov registry record
Phenotype/Genotype Correlations in Movement Disorders
A clinical trial of Movement Disorder, sponsored by National Institute of Neurological Disorders and Stroke (NINDS).
- Recruiting
- Registry status
- 2,500
- Enrollment target
- 1
- Study location
NCT00018889 is a study of Movement Disorder that is actively recruiting participants, run by National Institute of Neurological Disorders and Stroke (NINDS). The registered enrollment target is 2,500 participants, below the 4,124-participant average among 6 other Movement Disorder trials with a reported enrollment target (39% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00018889, a study of Movement Disorder, is actively recruiting participants, sponsored by National Institute of Neurological Disorders and Stroke (NINDS).
- RECRUITING
- Registry status
- 2,500 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this protocol is to identify families with inherited movement disorders and evaluate disease manifestations to establish an accurate clinical diagnosis by using newest technological advances and investigate the underlying molecular mechanisms. Studies of inherited movement disorders in large families with good genealogical records are especially valuable. Patients with diseases of known molecular basis will be genotyped in order to investigate phenotype/genotype correlation. Patients with disease of unknown or incomplete genetic characterization will be studied with a hope of contributing to the identification of specific disease-causing genes and genetic mechanisms responsible for a specific disorder.
Conditions Studied
Study Locations (1)
Maryland
- National Institutes of Health Clinical Center - Bethesda
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,500 participants |
| Start Date | 2001-10-22 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00018889
The ClinicalTrials.gov registry entry for NCT00018889 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 2,500 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,124-participant average among 6 other Movement Disorder trials with a reported enrollment target (39% lower). The listed sponsor is National Institute of Neurological Disorders and Stroke (NINDS), which has 567 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Movement Disorder appearing as the primary indexed condition, and to 0 interventions.
NCT00018889 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT00018889 about?
NCT00018889 is a clinical study titled "Phenotype/Genotype Correlations in Movement Disorders". The goal of this protocol is to identify families with inherited movement disorders and evaluate disease manifestations to establish an accurate clinical diagnosis by using newest technological advances and investigate the underlying molecular mechanisms. Studies of inherited movement disorders in l...
What is the current status of trial NCT00018889?
This trial is currently recruiting. The enrollment target is 2,500 participants. The study started on 2001-10-22.
What conditions does trial NCT00018889 study?
This clinical trial studies the following conditions: Movement Disorder.
Who is sponsoring clinical trial NCT00018889?
This trial is sponsored by National Institute of Neurological Disorders and Stroke (NINDS), which has 567 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00018889 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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