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Comparison of the Incidence of Dyskinesia in Parkinson's Disease Who Were Treated With Amantadine or Dopamine Agonist

A 10-year Observational Study of the Incidence of Dyskinesia in Patients With Early Parkinson's Disease Who Were Treated With Amantadine or Dopamine Agonist

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01338662
Enrollment
500
Registered
2011-04-19
Start date
2011-05-31
Completion date
2022-04-30
Last updated
2017-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's Disease

Keywords

Parkinson's disease

Brief summary

The purpose of this study is to compare the onset time and severity of dyskinesia in amantadine or Dopamine agonist initial treated groups in Parkinson's disease.

Detailed description

1. Dopamine agonist can delay the risk of dyskinesia by initiating treatment rather than levodopa. Amantadine is typical antidyskinetic drug. There is no data about comparison of risk of dyskinesia in amantadine and dopamine agonist by initiating treatment. 2. Prospective , randomized, open label study compare the onset time and severity of dyskinesia between groups randomized assigned order of amantadine and dopamine agonist

Interventions

None listed

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* 30\<age\<60 * IPD * H & Y\<3

Exclusion criteria

* previous dopaminergic medication history * dyskinesia * Parkinson plus * clinically significant or unstable medical or surgical condition

Design outcomes

Primary

MeasureTime frameDescription
dyskinesia onsetup to 10 years from the start of durg (Amantadine or dopaimine agonsit)observe duration of onset of dyskinesia from initial treatment observe until 10 years

Secondary

MeasureTime frameDescription
UPDRS, severity of dyskinesia between groupsobserve duration of onset of dyskinesia from initial treatmentobserve duration of onset of dyskinesia from initial treatment observe until 10 years compare the UPDRS and severity of dyskinesia between groups

Countries

South Korea

Contacts

Primary ContactBeom S Jeon, MD, PhD
brain@snu.ac.kr82-2-2072-2876
Backup ContactYoung Eun Kim, MD
yeksl99@hanmail.net82-2-2072-1219

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026