At a glance
ClinicalIndex Comparison RecordN/ACompleted
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases
National Institute of Neurological Disorders and Stroke (NINDS)·observational·Posted Dec 10, 2002·Updated Mar 4, 2008
In Brief
An observational study for Movement Disorders and 4 related conditions. Completed, across 1 site.
Detailed 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 Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsMovement Disorders, Myoclonus, Nervous System Diseases, Tic Disorders, Tremor
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
1997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMar 1997
Study CompletionApr 2000
First PostedDec 2002
TodayJul 2026
First PostedDec 10, 2002
Enrollment StartMar 1, 1997
Study CompletionApr 1, 2000
TodayJul 2, 2026
Posted 23.6 years ago