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Science

Published 25 August 2026

Ibogaine Success Rate: Why There Isn't One

Where the figures clinics quote actually come from, why none of them is a rate, and what the published follow-up record shows instead.

There is no ibogaine success rate. A rate needs a defined group of treated people and a count of what happened to all of them, and no study has ever produced one. The most quoted figures come from a survey of the 88 people a single clinic could still reach out of 336 it had treated, in which 70 per cent had relapsed.

Somebody quoted you a number, and it probably came with a confident tone.

This page is about where such numbers come from, which is a more useful thing to know than the numbers themselves.

What a success rate would require

Three things, none of which exists for ibogaine.

A denominator. Everyone who was treated, not everyone who answered afterwards. The people who died, who became too unwell to reply, or who never wanted to hear from the clinic again all belong in the count.

A definition fixed in advance. Abstinence from what, measured how, for how long, starting when.

A follow-up period that does not move. Reporting whoever happens to be reachable at whatever moment produces a figure that shifts with the effort put into finding people.

Every published ibogaine outcome figure is missing at least one of these. Most are missing all three.

The number everyone quotes

The 70 per cent figure comes from a retrospective survey of 88 people treated at one clinic in Mexico between 2012 and 2015.

FindingShare of the 88
Never used opioids again30 per cent
Abstinent for more than six months at the survey41 per cent
Relapsed at some point70 per cent
Relapsed but using less than before48 per cent
Consumption unchanged17 per cent
Consumption increased6 per cent

Now the denominator above the denominator. The clinic had treated 336 people in that window. 285 could be contacted, 134 started the survey, and 88 remained after exclusions.

That is 26 per cent of the people treated. The authors say plainly that those who could not be contacted or declined may have had different outcomes, which may have inflated their estimates. Three of the five authors worked for the clinic, its owner among them, and the clinic funded the ethics application.

The figure most often quoted wrongly

The same paper reports 54 per cent abstinent for a year or more and 31 per cent for two years or more. Both are percentages of the 30 per cent who never used again, not of the sample.

On the sample they are roughly 16 and 9 per cent. Lifting them from the abstract without their denominator turns a small minority into a majority, and it happens constantly.

The same people, two headlines

A second paper analysed 73 of those same 88 respondents and reported that 59 of them, 81 per cent, were treatment responders.

So one dataset yields “70 per cent relapsed” and “81 per cent responded”. Both are accurate. A responder was anyone abstinent or using less than before; a relapse was any return to use at any point.

A clinic quoting the second figure and a critic quoting the first are describing the same eighty-eight people. Whenever you see an ibogaine success figure, the definition is doing more work than the number.

The best prospective evidence

Surveys ask people to remember. A prospective study follows them forward, which is harder and much more informative.

Thirty people treated in Baja California were followed for a year. The same cohort carries the withdrawal result, which is a stronger finding than this one and belongs beside it.

MonthPeople reachedReporting no opioid use in 30 days
12015
31910
6146
91711
12147

Improvement was greatest at one month and, in the authors’ words, never again reached that level. Twelve of the thirty met their definition of a favourable outcome at nine or twelve months.

Look at the middle column. The count of people actually reached moves up and down, because which people could be found changed each round.

The authors ran the comparison both ways, and it matters which one is quoted. Against where people started, the improvement stayed significant throughout. Against the first month’s own standard, their non-inferiority test returned no significant result at any later point once missing data were accounted for. Their own reading is that a subset responded and kept responding, rather than that the group as a whole did.

A New Zealand cohort of fifteen found roughly half using opioids again at three, six and twelve months. Its three dropouts had all relapsed. One participant died during treatment.

Why the biggest series cannot help

The largest medically monitored series, 191 patients in St Kitts, is often cited as evidence of effectiveness.

It reports no drug use outcome at all. What it measured was mood, craving and physician-rated withdrawal, and at one month those measures existed for roughly a third of the participants. Its author declares that she founded and holds shares in a company developing ibogaine and holds patents on its active metabolite.

It is a genuine safety observation. It is not a success rate and was never designed to be one.

What the whole literature amounts to

A systematic review counted 24 studies covering 705 people: seventeen open-label studies or case series, three case reports, one retrospective survey, and three controlled studies, none of which tested ibogaine for efficacy in dependence. Two deaths occurred within those 24 studies.

That is the entire human evidence base from which success rates are quoted.

The comparison that actually decides something

People weighing this are usually not choosing between ibogaine and nothing. They are choosing between ibogaine and staying on an opioid agonist, and that comparison has been measured, on the other side.

Across 749,634 people, all-cause mortality during agonist treatment was less than half what it was out of treatment. In the four weeks after stopping, all-cause mortality ran about six times higher than during treatment, and stayed around double for as long as people remained off it.

This is the asymmetry to hold on to

On one side, a treatment whose effect on death has been measured in three quarters of a million people. On the other, a treatment whose effect on death has never been measured at all, and whose best outcome figure describes a quarter of one clinic’s patients.

That is not an argument that ibogaine does not work. Nobody can make that argument either, for the same reason. It is an argument that the two claims are not the same kind of claim.

The comparison has never been run directly. Iboga compared sets out what is known about each alternative separately.

If someone quotes you a figure

Four questions dismantle almost any of them.

  1. Out of how many treated? Not how many answered.
  2. Success defined as what? Abstinence, or reduced use, or getting through withdrawal.
  3. Measured when, and by whom? Self-report to the clinic that treated you is not a neutral measurement.
  4. Who is missing? In every study here, the people not reached are the ones whose outcomes would move the number most.

The honest answer to “does it work” is that detoxification appears to work in the short term, that a minority of people in small studies were doing better a year later, that nobody has counted the rest, and that two randomised trials finished in 2024 without reporting.

When it does not work covers what the follow-up record says about the people for whom it did not.

Common questions

There is no established rate. Every quoted figure comes from a survey or case series with no complete denominator, so it describes the people who answered rather than the people who were treated.

A retrospective survey of 88 people treated at one clinic in Mexico. It found 70 per cent had relapsed at some point and 30 per cent had never used opioids again.

Because most cite short-term detoxification success, which is the part least in dispute, or count only the people who responded to a follow-up request. Neither is a rate.

Nobody knows, because the comparison has never been made in humans. What is known is that mortality during agonist treatment is less than half what it is off treatment.

A randomised trial reporting drug use would go a long way. Two randomised trials completed in 2024 and neither has reported.

Sources

7 sources · How we source

  1. Subjective effectiveness of ibogaine treatment for problematic opioid consumption

    Primary source · Journal of Psychedelic Studies, 2017 · accessed 25 Aug 2026

  2. Treatment of opioid use disorder with ibogaine: detoxification and drug use outcomes

    Primary source · The American Journal of Drug and Alcohol Abuse, 2018 · accessed 25 Aug 2026

  3. A Mixed Method Analysis of Persisting Effects Associated with Positive Outcomes Following Ibogaine Detoxification

    Primary source · Journal of Psychoactive Drugs, 2018 · accessed 25 Aug 2026

  4. Ibogaine treatment outcomes for opioid dependence from a twelve-month follow-up observational study

    Primary source · The American Journal of Drug and Alcohol Abuse, 2018 · accessed 25 Aug 2026

  5. Association of Opioid Agonist Treatment With All-Cause Mortality and Specific Causes of Death Among People With Opioid Dependence

    Primary source · JAMA Psychiatry, 2021 · accessed 25 Aug 2026

  6. Ibogaine Detoxification Transitions Opioid and Cocaine Abusers Between Dependence and Abstinence

    Primary source · Frontiers in Pharmacology, 2018 · accessed 25 Aug 2026

  7. A systematic literature review of clinical trials and therapeutic applications of ibogaine

    Primary source · Journal of Substance Abuse Treatment, 2022 · accessed 25 Aug 2026

Portrait of Kathryn A. Cunningham

Kathryn A. Cunningham

Scientific review 25 August 2026

About

Professor and vice chair of pharmacology and toxicology at the University of Texas Medical Branch, Chauncey Leake Distinguished Professor of Pharmacology, and director of the Center for Addiction Sciences and Therapeutics. A behavioural neuropharmacologist by training, she works on the receptor pharmacology of substance use disorder and on turning that work into candidate treatments, which is the ground the pharmacology and addiction pages on this site stand on. Disclosure: UTMB Health is a partner in the public-university consortium awarded $50 million by the State of Texas in December 2025 to run ibogaine clinical trials, a programme this site covers.

  • Behavioural neuropharmacology
  • Addiction science
  • Serotonin receptor pharmacology
  • Substance use disorder therapeutics

On this page

  • What a success rate would require
  • The number everyone quotes
  • The same people, two headlines
  • The best prospective evidence
  • Why the biggest series cannot help
  • What the whole literature amounts to
  • The comparison that actually decides something
  • If someone quotes you a figure

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