drugset / Trial / NCT03187353

IMProving Executive Function Study

NCT03187353

Phase 4 Completed 69 enrolled University of Pennsylvania
RandomizedCrossoverTriple-blindTreatment

Summary

This is a double-blind, placebo-controlled, crossover study testing whether Vyvanse (lisdexamfetamine; LDX) improves executive functioning (EF) in 100 postmenopausal women who report onset of EF difficulties after oophorectomy. This study involves magnetic resonance imaging (MRI) to see how LDX affects brain chemistry while undergoing two 6-week trials of the study drug and placebo capsules. UPDATE: We have recently updated this protocol (09/2020) to offer a remote version of the study that can be completed entirely from the participant's home. This alternate version of the study eliminates travel, the MRI, and blood draws.

Timeline

Start
2017-09-22
Primary completion
2022-04-30
Completion
2022-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Lisdexamfetamine Other / unclassified 60 mg

Indications