# Phenotype/Genotype Correlations in Movement Disorders

> **NCT00018889** · — · RECRUITING · sponsor: **National Institute of Neurological Disorders and Stroke (NINDS)** · enrollment: 2500 (estimated)

## Conditions studied

- Movement Disorder

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT00018889
- **Lead sponsor:** National Institute of Neurological Disorders and Stroke (NINDS)
- **Sponsor class:** NIH
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** RECRUITING
- **Start date:** 2001-10-22
- **Primary completion:** —
- **Final completion:** —
- **Target enrollment:** 2500 (ESTIMATED)
- **Last updated:** 2026-05-04


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00018889

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00018889, "Phenotype/Genotype Correlations in Movement Disorders". Retrieved via AI Analytics 2026-06-12 from https://api.ai-analytics.org/clinical/NCT00018889. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*
