Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00682513 · ClinicalTrials.gov registry record

Studies of the Variable Phenotypic Presentations of Rapid-Onset Dystonia Parkinsonism and Other Movement Disorders

A clinical trial of Dystonia and Parkinsonism, sponsored by State University of New York at Buffalo.

Recruiting
Registry status
198
Enrollment target
2
Study locations

NCT00682513: Recruiting study of Dystonia and Parkinsonism, sponsored by State University of New York at Buffalo.

NCT00682513 is a study of Dystonia and Parkinsonism that is actively recruiting participants, run by State University of New York at Buffalo. The registered enrollment target is 198 participants, below the 533-participant average among 28 other Dystonia trials with a reported enrollment target (63% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00682513, a study of Dystonia and Parkinsonism, is actively recruiting participants, sponsored by State University of New York at Buffalo.

RECRUITING
Registry status
198 participants
Enrollment target
2
Study locations

Study Summary

The purposes of this study are to identify persons with rapid-onset dystonia-parkinsonism (RDP) or mutations of the RDP gene, document prevalence of the disease, and map its natural history.

Primary Outcome

History of symptom onset and duration will be obtained and current degree of severity assessed.

Conditions Studied

Study Locations (2)

Florida

  • University of Miami - Miami

New York

  • University at Buffalo - Buffalo

Trial Details

FieldValue
Enrollment Target 198 participants
Start Date 2008-04
Est. Completion 2027-07-31

What NCT00682513 shows while recruiting

NCT00682513 is an observational study that tracks outcomes without assigning an intervention. The registered 198 participants enrollment target is mid-sized for trials with a published cap, below the 533-participant average among 28 other Dystonia trials with a reported enrollment target (63% lower).

The record links to 2 conditions, with Dystonia appearing as the primary indexed condition, and to 0 interventions.

NCT00682513 reports a single indexed study location in Florida, New York.

Frequently Asked Questions

What is clinical trial NCT00682513 about?

NCT00682513 is a clinical study titled "Studies of the Variable Phenotypic Presentations of Rapid-Onset Dystonia Parkinsonism and Other Movement Disorders". The purposes of this study are to identify persons with rapid-onset dystonia-parkinsonism (RDP) or mutations of the RDP gene, document prevalence of the disease, and map its natural history.

What is the current status of trial NCT00682513?

This trial is currently recruiting. The enrollment target is 198 participants. The study started on 2008-04. Estimated completion is 2027-07-31.

What conditions does trial NCT00682513 study?

This clinical trial studies the following conditions: Dystonia, Parkinsonism.

Who is sponsoring clinical trial NCT00682513?

This trial is sponsored by State University of New York at Buffalo, which has 243 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00682513 being conducted?

This trial has 2 study locations across Florida, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Dystonia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00682513's enrollment target sits among peer trials

198 9th of 28 higher than 20 of 28 other Dystonia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Dystonia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05203328 · 198 participants · NA

    Prospective Study to Evaluate High Flow Nasal Cannula With Monitored Anesthesia Care During EBUS Bronchoscopy

  • NCT05426967 · 198 participants · NA

    rTMS for Military TBI-related Depression

  • NCT05561114 · 198 participants · Phase 3

    Paclitaxel Coated Balloon for the Treatment of Chronic bEnigN sTricture- Esophagus

  • NCT05585190 · 198 participants · NA

    Stand Up for Your Health with a Sit-stand Desk

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00682513, the US trial registry maintained by the National Library of Medicine. NCT00682513 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.