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NCT00001667 · ClinicalTrials.gov registry record

Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases

A clinical trial of Movement Disorders and Nervous System Diseases, sponsored by National Institute of Neurological Disorders and Stroke (NINDS).

Completed
Registry status
300
Enrollment target
1
Study location

NCT00001667 is a study of Movement Disorders and Nervous System Diseases that has completed, run by National Institute of Neurological Disorders and Stroke (NINDS). The registered enrollment target is 300 participants, below the 1,056-participant average among 26 other Movement Disorders trials with a reported enrollment target (72% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00001667, a study of Movement Disorders and Nervous System Diseases, has completed, sponsored by National Institute of Neurological Disorders and Stroke (NINDS).

COMPLETED
Registry status
300 participants
Enrollment target
1
Study location

Study Summary

The purpose of this protocol is to identify families with inherited neurologic conditions, especially movement disorders, to evaluate affected and unaffected individuals clinically, and to obtain blood samples for genetic analysis.

Study Locations (1)

Maryland

  • National Institute of Neurological Disorders and Stroke (NINDS) - Bethesda

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 1997-03
Est. Completion 2000-04

What the Registry Record Tells You About NCT00001667

The ClinicalTrials.gov registry entry for NCT00001667 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,056-participant average among 26 other Movement Disorders trials with a reported enrollment target (72% 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 5 conditions, with Movement Disorders appearing as the primary indexed condition, and to 0 interventions.

NCT00001667 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT00001667 about?

NCT00001667 is a clinical study titled "Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases". The purpose of this protocol is to identify families with inherited neurologic conditions, especially movement disorders, to evaluate affected and unaffected individuals clinically, and to obtain blood samples for genetic analysis.

What is the current status of trial NCT00001667?

This trial is currently completed. The enrollment target is 300 participants. The study started on 1997-03. Estimated completion is 2000-04.

What conditions does trial NCT00001667 study?

This clinical trial studies the following conditions: Movement Disorders, Nervous System Diseases, Tremor, Tic Disorders, Myoclonus.

Who is sponsoring clinical trial NCT00001667?

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 NCT00001667 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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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