North American Prodromal Synucleinopathy Consortium

NCT03623672 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2024-11-06

No results posted yet for this study

Summary

This study will enroll participants with idiopathic rapid eye movement (REM) sleep behavior disorder (RBD), for the purpose of preparing for a clinical trial of neuroprotective treatments against synucleinopathies.

Conditions

  • REM Sleep Behavior Disorder
  • Parkinson Disease
  • Lewy Body Disease
  • Dementia With Lewy Bodies
  • Multiple System Atrophy
  • REM Sleep Parasomnias

Sponsors & Collaborators

Principal Investigators

  • Yo-El Ju, MD · Washington University School of Medicine

  • Bradley Boeve, MD · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-29
Primary Completion
2026-07-31
Completion
2026-07-31

Countries

  • United States
  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03623672 on ClinicalTrials.gov