CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 11 enrolled
Drug / intervention
Methylphenidatedrug
Likely dose
Methylphenidate 30 mgfrom 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/NCT02225106
NCT02225106Phase 2Completed

Dopamine Receptor Imaging to Predict Response to Stimulant Therapy in Chronic TBI

University of Pennsylvania·interventional·Posted Aug 26, 2014·Updated Nov 15, 2019

In Brief

A Phase 2 clinical trial evaluating Methylphenidate for Cognition Disorder and 2 related conditions. Completed, enrolled 11 participants across 1 site.

Detailed Summary

Deficits in memory, attention, cognitive, and executive functions are the most common disabilities after traumatic brain injury (TBI). Dopamine (DA) neurotransmission is implicated in these neural functions and dopaminergic pathways are recognized to be frequently disrupted after TBI. Methylphenidate increases synaptic DA levels by binding to presynaptic dopamine transporters (DAT) and blocking re-uptake. The objectives of this study are to use PET imaging with \[11C\]-raclopride, a D2/D3 receptor ligand, before and after administering methylphenidate, to measure endogenous DA release in patients who are experiencing problems with cognition, attention and executive function in the chronic stage after TBI. In addition, we will use TMS to test short intracortical inhibition, a gamma-aminobutyric acid receptor A (GABAA) - mediated phenomenon, which is under partial DA control, as a measure of dopaminergic activity on and off

Study Details

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

Timeline

Phase 2CompletedFinished
201520162017201820192020202120222023202420252026
First PostedAug 26, 2014
Enrollment StartAug 6, 2014
Primary CompletionJun 21, 2017
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 11.8 years ago

Interventions

Methylphenidatedrug

Subjects will be treated with oral methylphenidate, using a forced titration up to a dose of 30 mg given twice daily for 4 weeks. At that point, the neuropsychologic tests are repeated.