CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 15 enrolled
Drug / intervention
Morphine +1 moredrug
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/NCT01878006
NCT01878006Phase 2Completed

OPRM1 A118G SNP Effect on Striatal Dopamine Response to an IV Opiate

National Institute on Alcohol Abuse and Alcoholism (NIAAA)·interventional·Posted Jun 14, 2013·Updated Apr 1, 2021

In Brief

A Phase 2 clinical trial evaluating Morphine and Placebo for Polymorphism-Genetic and 2 related conditions. Completed, enrolled 15 participants across 1 site.

Detailed Summary

Background: \- Small differences in genes may alter responses to drugs. One gene that has different forms is the mu opioid receptor gene. People with one form of this gene are more sensitive to alcohol. People with a different form are sometimes more sensitive to pain. Morphine and other prescription pain pills produce pain relief by acting at the mu opioid receptor. Researchers want to see the effect of morphine on brain reward and subjective effects. Morphine is a strong but short-acting pain medication that is sometimes used for anesthesia during surgery. Objectives: \- To compare the effect of morphine on brain measures of dopamine release using imaging. Eligibility: \- Individuals between 21 and 55 years of age who have previously taken pain pills prescribed to treat pain from a medical or dental procedure. Design: * This study has a screening phase and a study phase. The screening phase involves one or two visits of 5 to 6 hours. The study phase consists of 4 study visits. Each study visit will take about 8 hours. * Participants will be screened with a medical and psychiatric history and physical exam. They will be asked about drinking and drug-taking history, and any family history of alcoholism or drug abuse. Blood, urine, and breath samples will be collected. * During the first study visit, an MRI scan may be performed, questionnaires completed, and a blood sample collected for genetic testing. * During study visit 2, participants will test their pain sensitivity by placing one hand in cold water. Pupil diameter will be measured after the sensitivity test. After a blood sample is taken, participants will receive the morphine or a salt solution. The sensitivity test and pupil diameter test will be repeated. Final blood samples will be collected. A brief physical exam will also be performed. * During study visits 3 and 4, participants will receive morphine or a salt solution during a PET scan. Questionnaires to assess subjective effects will be administered. Final blood samples will be collected. A brief physical exam will also be performed. * Participants will stay in the clinic until the effects of the drug have worn off after study visits 2, 3, and 4. * About 1 week after the study session, participants will have a follow-up phone call.

Study Details

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

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJun 14, 2013
Enrollment StartJun 13, 2013
Primary CompletionApr 27, 2017
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 13.0 years ago

Interventions

Morphinedrug

Placebodrug