Your session is about to expire
← Back to Search
Benzodiazepine
Opioids + Benzodiazepines for Substance Abuse (MAP Trial)
Phase 2
Recruiting
Led By Mark K Greenwald, PhD
Research Sponsored by Wayne State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
Past-month benzodiazepine or opioid prescription (which would suggest daily use, tolerance, or withdrawal upon cessation)
Meet DSM-5 criteria for current psychosis, bipolar disorder, or severe depression
Timeline
Screening 3 weeks
Treatment Varies
Follow Up difference from placebo condition, measured within each session at 15-240 min post-drug 2 administration; measured in each of the 6 laboratory sessions over about 3 weeks
Summary
This trial will study the effects of opioids and benzodiazepines on cognition, emotions, and behavior.
Who is the study for?
This trial is for adults who have used opioids and sedatives in the past five years, not seeking treatment, and are generally healthy. They may have mild to moderate opioid or sedative use disorder but can't be severely overweight, pregnant, using certain drugs, or have severe mental health issues.
What is being tested?
The study tests how morphine (an opioid) and alprazolam (a benzodiazepine) affect emotions, thinking, and behavior when taken alone or together compared to a placebo. It aims to understand the impact of these substances on chronic users.
What are the potential side effects?
Possible side effects include drowsiness, confusion, addiction potential with long-term use; slowed breathing; impaired coordination; mood changes; memory problems; risk of overdose especially when combined.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have been prescribed benzodiazepines or opioids in the past month.
Select...
I have been diagnosed with psychosis, bipolar disorder, or severe depression.
Select...
I am not pregnant, breastfeeding, or if sexually active, I use birth control.
Select...
I am currently taking methadone, buprenorphine, or naltrexone.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ difference from placebo condition, measured within each session at 15-240 min post-drug 2 administration; measured in each of the 6 laboratory sessions over about 3 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~difference from placebo condition, measured within each session at 15-240 min post-drug 2 administration; measured in each of the 6 laboratory sessions over about 3 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Negative affect
Positive affect
State anxiety
Secondary study objectives
Blood pressure
Cognitive flexibility performance task
Cognitive inhibition performance task
+13 moreTrial Design
6Treatment groups
Active Control
Placebo Group
Group I: Alprazolam then morphineActive Control2 Interventions
0.25mg oral alprazolam administered at 9:30 am, then 15mg oral morphine administered at 12:00 pm
Group II: Morphine aloneActive Control1 Intervention
15mg immediate-release oral morphine, administered both at 9:30 am and 12:00 pm
Group III: Alprazolam aloneActive Control1 Intervention
0.25mg oral alprazolam, administered at both 9:30 am and 12:00 pm
Group IV: Morphine then alprazolamActive Control2 Interventions
15mg oral morphine administered at 9:30 am, then 0.25mg oral alprazolam administered at 12:00 pm
Group V: Morphine+alprazolam simultaneouslyActive Control2 Interventions
morphine 15mg + 0.25mg alprazolam at 9:30 am, then morphine 15mg + 0.25mg alprazolam at 12:00 pm
Group VI: Placebo drugPlacebo Group1 Intervention
Lactose, administered both at 9:30 am and 12:00 pm
Find a Location
Who is running the clinical trial?
Wayne State UniversityLead Sponsor
314 Previous Clinical Trials
110,054 Total Patients Enrolled
Henry Ford Health SystemOTHER
311 Previous Clinical Trials
2,176,342 Total Patients Enrolled
1 Trials studying Opioid Addiction
200 Patients Enrolled for Opioid Addiction
Mark K Greenwald, PhDPrincipal InvestigatorWayne State University
5 Previous Clinical Trials
177 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have been prescribed benzodiazepines or opioids in the past month.I have used opioids or sedatives in the past 5 years and may currently have a mild to moderate addiction to them.I have used opioids or sedatives in the last 10 years, for any reason.I have been diagnosed with psychosis, bipolar disorder, or severe depression.I have a condition affecting my nervous, heart, lung, or other body systems.I am not pregnant, breastfeeding, or if sexually active, I use birth control.I am currently taking methadone, buprenorphine, or naltrexone.I haven't taken any forbidden medications in the last 30 days.
Research Study Groups:
This trial has the following groups:- Group 1: Alprazolam then morphine
- Group 2: Placebo drug
- Group 3: Morphine alone
- Group 4: Alprazolam alone
- Group 5: Morphine then alprazolam
- Group 6: Morphine+alprazolam simultaneously
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger