Efficacy and Safety of Rasagiline in Prodromal Parkinson's Disease

NCT05611372 · Status: WITHDRAWN · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL

Last updated 2025-01-07

No results posted yet for this study

Summary

To investigate whether a year of rasagiline may reduce the progression from idiopathic REM sleep behavior disorder (RBD) to Parkinson's disease (PD).

Conditions

  • REM Sleep Behavior Disorder
  • Parkinson Disease
  • Synucleinopathies

Interventions

DRUG

Rasagiline

1 mg rasagiline

Sponsors & Collaborators

  • Beijing Tiantan Hospital

    collaborator OTHER
  • Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

    collaborator OTHER
  • Jiangsu Province Nanjing Brain Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Anhui Medical University

    collaborator OTHER
  • Huashan Hospital

    collaborator OTHER
  • Second Affiliated Hospital of Soochow University

    collaborator OTHER
  • Guizhou Medical University

    collaborator OTHER
  • The First Affiliated Hospital of Guangzhou Medical University

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Sir Run Run Shaw Hospital

    collaborator OTHER
  • The Affiliated Hospital of Hangzhou Normal University

    collaborator OTHER
  • The First Affiliated Hospital of Dalian Medical University

    collaborator OTHER
  • Qilu Hospital of Shandong University

    collaborator OTHER
  • Fujian Medical University Union Hospital

    collaborator OTHER
  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    lead OTHER

Principal Investigators

  • Baorong Zhang, MD · Second Affiliated Hospital, Zhejiang University, China

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2025-12-31
Completion
2026-12-31

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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 NCT05611372 on ClinicalTrials.gov