Opioid use disorder affects millions in the US, driven by prescription painkillers, heroin, and synthetic opioids like fentanyl. Current treatment centers on medications like buprenorphine, methadone, and naltrexone, combined with counseling. Despite these tools, relapse rates remain high and overdose deaths continue to climb.
What's actually going on in research
Trials are testing longer-acting formulations that reduce the burden of daily dosing, vaccines that block opioid effects in the brain, and new medications targeting different brain pathways. Researchers are also studying how to improve access to treatment, prevent overdose deaths, and address co-occurring mental health conditions like depression and trauma.
Long-acting medications
Monthly and six-month injections of buprenorphine are being tested to replace daily pills or films. These formulations may improve adherence and reduce diversion risk.
Opioid vaccines
Vaccines in development teach the immune system to trap opioids before they reach the brain. Early trials are testing whether this approach can prevent relapse and overdose.
Treatment delivery models
Studies are testing telemedicine prescribing, pharmacy-based treatment initiation, and emergency department programs. The goal is to reach people faster and reduce barriers to starting medication.
What to know before you search
Eligibility typically depends on diagnosis of opioid use disorder, current substance use patterns, prior treatment history, and willingness to participate in counseling or monitoring.
What types of trials are currently open
- Medication trials — Testing new formulations of buprenorphine, naltrexone, or entirely new drugs that target addiction pathways in the brain.
- Vaccine trials — Testing vaccines that prevent opioids from entering the brain and producing euphoria or respiratory depression.
- Treatment access studies — Comparing different ways to deliver medication treatment, such as through primary care, pharmacies, or telehealth.
- Overdose prevention trials — Testing strategies to prevent overdose deaths, including supervised consumption sites and expanded naloxone distribution.
- Behavioral intervention studies — Testing counseling approaches, peer support programs, and contingency management to support recovery alongside medication.
Recently added Opioid Use Disorder trials
Applying Low-Intensity Focused Ultrasound in Treating Severe Substance Use Disorder: Tolerability and Effectiveness
The goal of this clinical trial is to investigate the safety and efficacy of applying low-intensity focused ultrasound targeting the nucleus accumbens in individuals with opioid or amphetamine use disorders. The main questions it aims to answer is: \- Low-intensity focused ultrasound targeting the nucleus accumbens demonstrates sufficient safety and predictable therapeutic efficacy in individuals with opioid or amphetamine use disorders. Participants will: * Received Low-intensity focused ultrasound neuromodulation once * Visit the clinic for checkups and asessment at 1 week, 1 month, 3 months, 6 months, 9 months, 1 year, 1.5 years, and 2 years after received Low-intensity focused ultrasound neuromodulation.
Mindfulness Texting for Medication Adherence and Chronic Pain Management
The goal of this clinical trial is to examine the effects of reminder and mindfulness text messages based on integrated Acceptance and Commitment Therapy and Mindfulness Based Relapse Prevention (ACT+MBRP) on medication adherence and managing craving, pain, mindfulness, and withdrawal symptoms in people taking medications for opioid use disorder and with chronic pain through assessment questions collected six times daily during the course of treatment. The main questions it aims to answer are: 1. Do daily medication reminder text messages increase medication adherence for people taking medications for opioid use disorder? 2. To what extent do people engage with the daily mindfulness messages? 3. Do participants receiving a structured curriculum of mindfulness messages delivered twice daily differ from those receiving randomly selected mindfulness messages delivered four times daily in engagement with the intervention? 4. How do the two mindfulness text messaging interventions differ in their effects on intervention engagement, craving, pain, mindfulness, and withdrawal symptoms? Participants will: 1. Receive daily medication reminder text messages for 12 weeks (i.e., 3 months) 2. Receive either 2 or 4 mindfulness messages per day for 6 weeks 3. Answer brief assessment questions six times per day during the 6-week mindfulness text messaging period 4. Complete questionnaires at enrollment (baseline), once each week during the 6-week mindfulness text messaging period (6 total), immediately after the 6-week mindfulness text messaging period (post-treatment), and 6 weeks after the mindfulness text messaging period ends (follow-up)
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