Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01256905

Attention Modulation for Treatment of Parkinson's Disease and Dementia With Lewy Bodies

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
NYU Langone Health · Academic / Other
Sex
All
Age
50 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate if a drug commonly used to treat excessive day-time sleepiness, called armodafinil (Nuvigil), is also effective in improving the impairment in the attention commonly reported by patients with more advanced Parkinson's disease (PD) and Lewy body disease (LBD).

Detailed description

The main aims of this study are: 1\. To investigate whether in PDD and DLB th specific disturbances in the basal ganglia thalamocortical network, measured through the Electroencephalography (EEG) frequency analysis, are ameliorated by armodafinil. Our main hypothesis is that armodafinil can restore the attention and improve cognitive disturbances in PDD and DLB, through a specific effect on striatal-thalamo-cortical activity.

Conditions

Interventions

TypeNameDescription
DRUGArmodafinilArmodafinil 150 mg

Timeline

Start date
2011-01-01
Primary completion
2011-08-08
Completion
2011-08-08
First posted
2010-12-09
Last updated
2021-08-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01256905. Inclusion in this directory is not an endorsement.

Attention Modulation for Treatment of Parkinson's Disease and Dementia With Lewy Bodies (NCT01256905) · Clinical Trials Directory