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Clinical Trial Summary

The purpose of this study is to see whether the ICDs(Impulse Control Disorder) are improved and neuropsychiatric traits related to ICD are changed or not when switching dopamine agonist to levodopa/carbidopa in patients with Parkinson's disease who have been treated with dopaminergic medications.


Clinical Trial Description

- PRIMARY OBJECTIVE To evaluate the improvement of mMIDI(modified version of Minnesota Impulsive Disorders Interview,Korean version) score from the baseline to 12 weeks or LOCF(Last Observation Carried Forward) - SECONDARY OBJECTIVE i) To evaluate the improvement of neuropsychiatric profiles from the baseline to 12 weeks or LOCF ii) To evaluate the improvement of UPDRS(Unified Parkinson's Disease Rating Scale)Score from the baseline to 12 weeks or LOCF ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01683253
Study type Interventional
Source Sandoz
Contact
Status Completed
Phase Phase 4
Start date November 2012
Completion date December 2014

See also
  Status Clinical Trial Phase
Active, not recruiting NCT02927002 - Effects of Non-invasive Brain Stimulation in Impulse Control Disorders N/A
Completed NCT01052831 - Naltrexone for Impulse Control Disorders in Parkinson's Disease Phase 4
Recruiting NCT06237868 - rTMS Over the Dorsolateral Prefrontal Cortex for the Treatment of Impulse Control Disorders in Parkinson's Disease N/A
Recruiting NCT05712057 - Neurostimulation Versus Therapy for Problems With Emotions N/A
Recruiting NCT03146130 - Study of the Efficacy of N-acetylcysteine (NAC) on Impulse Control Disorders Phase 3