Is naltrexone suitable?
Current opioid use, recent opioid exposure, pregnancy, liver history, other medicines, and mental health can change the risk-benefit decision.
Evidence reviewed
Evidence review
The Sinclair Method is a popular name for targeted naltrexone taken in relation to planned drinking. Trials support targeted dosing as a possible alcohol-reduction option for selected people, but the evidence does not justify a universal 78% success rate or a guaranteed extinction timeline.

Targeted naltrexone means taking prescribed naltrexone in anticipation of a higher-risk drinking situation rather than automatically taking it every day. The name “Sinclair Method” is widely used online, but it is not a separate medicine or a single globally standardised protocol.
Randomized trials have found benefit on some drinking outcomes in selected groups. They do not establish that 78% of everyone treated succeeds, that abstinence treatment fails 60–90% of the time, or that most people reach “extinction” within a fixed number of months. Daily naltrexone also has a substantial evidence base and remains the labelled or guideline-supported approach in many settings.
| Study | Design | What it found | Important limit |
|---|---|---|---|
| Heinälä et al., 2001 | 121 people; naltrexone or placebo with coping-skills or supportive therapy | During 12 weeks of daily treatment, naltrexone plus coping skills reduced relapse to heavy drinking; a 20-week targeted phase followed | The often-repeated “78% success” claim is not the trial result |
| Santos et al., 2022 | 120 sexual and gender minority men with mild-to-moderate AUD; targeted 50 mg naltrexone or placebo for 12 weeks | Naltrexone reduced binge-drinking days and several secondary drinking outcomes | A specific population and short treatment period; not proof of the same effect for everyone |
Targeted dosing is a treatment decision, not a do-it-yourself drinking rule.
Current opioid use, recent opioid exposure, pregnancy, liver history, other medicines, and mental health can change the risk-benefit decision.
Reduced heavy drinking, abstinence, craving, and treatment retention are different outcomes. Agree on measures and a review date.
The evidence and local product label may support different approaches. The plan should account for adherence and the likelihood of unplanned drinking.
Decide what happens after a missed dose, opioid pain emergency, worsening drinking, adverse effects, or no meaningful improvement.
Daily treatment followed by a targeted phase; 121 participants.
Targeted oral naltrexone in 120 sexual and gender minority men.
Contraindications and opioid-overdose warnings.
Bring the trial links and your treatment goals to a licensed clinician. Ask how the evidence applies to you and how progress and safety will be monitored.