Viewing Study NCT01673594


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Study NCT ID: NCT01673594
Status: COMPLETED
Last Update Posted: 2016-11-30
First Post: 2012-06-21
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Prevention of Stimulant-Induced Euphoria With an Opioid Receptor Antagonist
Sponsor: Massachusetts General Hospital
Organization:

Study Overview

Official Title: Prevention of Stimulant-Induced Euphoria With an Opioid Receptor Antagonist
Status: COMPLETED
Status Verified Date: 2016-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to a) assess the efficacy of naltrexone in preventing stimulant-induced euphoria in adults with ADHD, b) assess whether naltrexone will interfere with the clinical efficacy of stimulants in treating adults with ADHD, c) assess whether naltrexone will interfere with the effects of stimulants on neurotransmitter activity. We predict that naltrexone will successfully prevent stimulant-induced euphoria without interfering with the ability of stimulants to effectively treat ADHD in adults. This study will be an 8 -week trial with young adults (18-24) with ADHD.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: