Your session is about to expire
← Back to Search
Opioid Agonist
Methadone Dosing for Opioid Use Disorder
Phase 2
Recruiting
Led By Denis Antoine, MD
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Aged 18 years of age or older
Currently receiving methadone for treatment of OUD for >90 days and have been consuming the same dose for >30 days
Must not have
Presence of acute medical problem that requires immediate and intense medical management
Currently receiving split doses of methadone
Timeline
Screening 3 weeks
Treatment Varies
Follow Up weeks 1, 6, and 12
Awards & highlights
No Placebo-Only Group
Summary
This trial will compare the effectiveness of two different methadone dosing schedules for people with both pain and an opioid use disorder.
Who is the study for?
This trial is for adults over 18 who have been on a stable methadone dose for opioid use disorder (OUD) treatment for at least 90 days. Participants must be willing to follow the study schedule, carry a phone during part of the study, and experience chronic pain. Pregnant individuals or those with acute medical issues, severe mental illness, or conditions that contraindicate split-dosing of methadone are excluded.
What is being tested?
The study is testing if taking methadone once daily versus twice daily can effectively manage both chronic pain and OUD. Participants will receive either their full dose all at once or half the dose twice a day to see which method works better.
What are the potential side effects?
Methadone may cause side effects such as drowsiness, dizziness, constipation, nausea, vomiting, sweating and changes in mood. The risk of side effects might vary depending on whether it's taken once or twice daily.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am 18 years old or older.
Select...
I have been on a stable dose of methadone for OUD for over 30 days.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am currently dealing with a serious health issue that needs urgent medical attention.
Select...
I am currently taking methadone in divided doses.
Select...
My methadone dose cannot be divided.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ weeks 1, 6, and 12
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~weeks 1, 6, and 12
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in worst pain rating- past 24 hour as assessed by the Brief Pain Inventory scale
Secondary study objectives
Change in Opioid Withdrawal Severity- past 24 hours as assessed by the Subjective Opioid Withdrawal Scale
Change in Pain Interference- past 7 days as assessed by Pain-related Disability Scale Total Score
Change in Pain Tolerance Latency
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Split-dosingExperimental Treatment1 Intervention
Participants in split dosing group will receive 50% active methadone + placebo twice daily.
Group II: Treatment as Usual (TAU)Active Control1 Intervention
Participants in treatment as usual group will receive 100% active methadone in AM + placebo in PM.
Find a Location
Who is running the clinical trial?
National Institute on Drug Abuse (NIDA)NIH
2,582 Previous Clinical Trials
3,326,890 Total Patients Enrolled
Johns Hopkins UniversityLead Sponsor
2,323 Previous Clinical Trials
14,874,157 Total Patients Enrolled
Denis Antoine, MDPrincipal InvestigatorJohns Hopkins University
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am 18 years old or older.I am on pain treatment where methadone split-dosing is not suitable.I have a cell phone or am willing to carry one provided by the study.I experience pain.You do not have a disability that falls within the mild to severe range, as determined by a specific definition that is not disclosed.I am currently dealing with a serious health issue that needs urgent medical attention.You are not planning to stop taking methadone during the study.I am currently taking methadone in divided doses.My methadone dose cannot be divided.I have been on a stable dose of methadone for OUD for over 30 days.You have taken methadone to bring home as part of your regular treatment.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment as Usual (TAU)
- Group 2: Split-dosing
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
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