Clinical Trials Directory

Trials / Completed

CompletedNCT01977625

LDX and Functional Magnetic Resonance Imaging (fMRI in Menopausal Women

Utilizing fMRI to Determine the Effects of Vyvanse® on Memory, Attention, and Brain Activity in Menopausal Women

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
18 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
Female
Age
45 Years – 60 Years
Healthy volunteers
Accepted

Summary

This study seeks to assess the effects of lisdexamfetamine (trademark name: Vyvanse; LDX) on executive function and prefrontal cortex activation in menopausal women ages 45-57, who report subjective cognitive difficulties. This protocol will recruit women from Dr. Epperson's ongoing study, Protocol #812470, to examine the impact of LDX on brain activation during performance of cognitive tasks specifically probing prefrontal cortex function.

Conditions

Interventions

TypeNameDescription
DRUGLisdexamfetamineThe overall objective of this study is to assess the effects of LDX on brain activation patterns during tasks of sustained attention and working memory in menopausal women.
OTHERPlaceboTo assess the effects of a placebo pill on brain activation patterns during tasks of sustained attention and working memory in menopausal women.

Timeline

Start date
2011-12-01
Primary completion
2014-04-01
Completion
2014-04-01
First posted
2013-11-06
Last updated
2018-07-27
Results posted
2017-07-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01977625. Inclusion in this directory is not an endorsement.