Brain scans reveal Ibogaine's effects on opioid cravings
NCT ID NCT07226570
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study uses brain scans (MRI, MRS, EEG) to see how ibogaine affects the brain in 20 people with moderate to severe opioid use disorder. Participants will already be receiving legal ibogaine treatment outside the U.S. The research team only observes and measures brain activity, cravings, and withdrawal symptoms before and after treatment. The goal is to understand how ibogaine might work in the brain, not to test if it is a safe or effective treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ibogaine
- What this could lead to
- If successful, this study could help explain how ibogaine affects the brain in opioid use disorder, potentially guiding future treatments.
- What could go wrong
- This is a very small observational study (20 people) where researchers do not provide the treatment. It cannot prove ibogaine works or is safe, only explore brain changes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults ages 21 to 70 with a confirmed diagnosis of moderate to severe opioid use disorder (OUD), defined as meeting four or more symptoms according to DSM-5 criteria. Participants must be independently scheduled to receive ibogaine treatment at a licensed clinic outside the United States.
- Ages
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21 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults aged 21-70 with confirmed moderate to severe OUD as assessed by equal or greater than 4 symptoms using DSM-5 criteria. * Independently scheduled to receive ibogaine treatment at Ambio Life Sciences in Tijuana, Mexico. * Able to undergo MRI and EEG procedures at UC Irvine at Visit 1 (baseline), Visit 4, and Visit 5, totaling three sessions. * Able to complete psychometric surveys at each study time point. * Able to provide urine samples at all three scanning sessions at UCI. * Able to provide urine samples at a local external lab for 3- and 6-month follow-ups. * Capable of giving written informed consent. * Proficient ability to speak, read, and write in English. Exclusion Criteria: * Presence of known past procedures, devices in the body, claustrophobia, or other contraindications for MRI. * Use of any psychedelic substances within 3 months prior to screening. * Diagnosis of schizophrenia, bipolar disorder (type I or II), or borderline personality disorder. * Use of ibogaine within 6 months prior to screening. * Pregnant or nursing. Participants who become pregnant during the study will be withdrawn from further participation. * Diagnosis of epilepsy or history of seizures. * Other contraindications to MRI/EEG methods. These may include but are not limited to: brain surgical clips and surgical staples, metal implants in the brain, and certain metallic dental material. * Inability to complete MRI/EEG sessions or follow-up visits. * Inability or unwillingness of an individual to give written informed consent. Note: UCI does not sponsor or financially support the ibogaine treatment in any way; all treatment costs are the sole responsibility of the participant.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Susan Samueli Integrative Health Institute, University of California, Irvine
RECRUITINGIrvine, California, 92617, United States
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