CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 12 enrolled
Drug / intervention
armodafinildrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00592943
NCT00592943Phase 2Completed

A PET Study Examining the Dopaminergic Activity of Armodafinil in Adults

Massachusetts General Hospital·interventional·Posted Jan 14, 2008·Updated Nov 13, 2013

In Brief

A Phase 2 clinical trial evaluating armodafinil for Healthy. Completed, enrolled 12 participants across 1 site.

Detailed Summary

The specific aims of this study are 1) to document the Dopamine Transporter (DAT) receptor occupancy of armodafinil using positron emission tomography (PET) scanning with C-11 altropane as the ligand and 2) to document the increased intrasynaptic dopamine produced by armodafinil using PET scanning with C-11 raclopride as the ligand. We hypothesize that DAT occupancy will be low with armodafinil; less than the DAT occupancy produced by therapeutic doses of methylphenidate. We also hypothesize that increases in intrasynaptic dopamine will be relatively low with armodafinil.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJan 14, 2008
Enrollment StartOct 1, 2007
Primary CompletionMay 1, 2008
Study CompletionMay 1, 2010
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 18.5 years ago

Interventions

armodafinildrug

tablet, taken by mouth, once each study day