Evidence map›Paper›PMID 40524244›Full record

ArticleAddiction science & clinical practice2025

High induction rate onto extended-release naltrexone for people with opioid use disorder: experiences from a Norwegian naturalistic study.

Jon Mordal, Farid Juya, Line Holtan, John-Kåre Vederhus, Arild Opheim, Ida H Brenna, Asle E Enger, Bente Weimand, Kristin Klemmetsby Solli, Lars Tanum

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Addiction science & clinical practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03647774 (Long Acting Naltrexone for Opioid Addiction), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03647774 phase4completednot on this map

Long Acting Naltrexone for Opioid Addiction: the Importance of Mental, Physical and Societal Factors for Sustained Abstinence and Recovery

TypeinterventionalSponsorLars TanumRan2018 to 2022Enrolled317ConditionsOpioid-use DisorderArmsExtended release naltrexone
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Jon MordalDivision of Mental Health and Addiction, Vestfold Hospital Trust, Tønsberg, 3103, Norway. jon.mordal@siv.no.
Farid JuyaDivision of Mental Health and Addiction, Vestfold Hospital Trust, Tønsberg, 3103, Norway.
Line HoltanDivision of Mental Health and Addiction, Vestfold Hospital Trust, Tønsberg, 3103, Norway.
John-Kåre VederhusAddiction Unit, Sørlandet Hospital HF, Kristiansand, 4604, Norway.
Arild OpheimDepartment of Addiction Medicine, Haukeland University Hospital, Østre Murallmenningen 7, Bergen, 5021, Norway.
Ida H BrennaDepartment of Addiction Medicine, Haukeland University Hospital, Østre Murallmenningen 7, Bergen, 5021, Norway.
Asle E EngerDepartment of Addiction Treatment, Oslo University Hospital, Oslo, 0424, Norway.
Bente WeimandMental Health Services, Akershus University Hospital, Lørenskog, 1478, Norway.
Kristin Klemmetsby SolliDivision of Mental Health and Addiction, Vestfold Hospital Trust, Tønsberg, 3103, Norway.
Lars TanumMental Health Services, Akershus University Hospital, Lørenskog, 1478, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor people with opioid use disorder (OUD), extended-release naltrexone (XR-NTX) is an effective antagonist treatment option. However, successful opioid tapering and abstinence is a prerequisite for XR-NTX induction and has repeatedly been reported as a major barrier to effective treatment. The aims of this study were to describe XR-NTX induction rates, reasons for incomplete induction, and extraordinary complications reported during the induction phase. We also compared sociodemographic and clinical variables among those who did and did not complete induction onto XR-NTX.

methodsThis naturalistic, multicenter, and open-label Norwegian study of XR-NTX included men and women aged 18-65 who had severe OUD. Most participants were referred to inpatient medically managed opioid withdrawal and received individualized pharmacological and psychosocial treatment according to clinical assessment and national guidelines. After opioid withdrawal, the participants underwent a minimum of three opioid-free days prior to XR-NTX induction. Variables were collected through baseline assessments and a retrospective patient chart review. XR-NTX induction completers and non-completers were compared via bivariate and logistic regression analyses.

resultsOf 129 participants with recent opioid use at inclusion, 106 (82%) completed XR-NTX induction. Induction was initiated in an inpatient setting for 116 participants (90%) and extraordinary complications were noted for 19 (15%) patients. Withdrawal symptoms and ambivalence were the most common reasons for non-completion, each noted in 75% of the cases. As compared with those who successfully completed induction, non-completers more often reported lifetime hepatitis (78% vs. 52%, p = 0.017), had a longer period of current substance use (mean 119 vs. 54 months, p = 0.001), and more frequently used methadone prior to study inclusion (43% vs. 8%, p < 001). In logistic regression analyses, methadone use was the only significant factor and was negatively associated with completion (odds ratio 0.20, 95% confidence interval = 0.05-0.72, p = 0.014).

conclusionThe results demonstrate the safety, efficacy and tolerability of a Norwegian opioid withdrawal and XR-NTX induction procedure. Although the present induction rate was high, our findings indicate that methadone users need special attention and tailored interventions regarding opioid withdrawal management and XR-NTX induction.

trial registrationThe study is registered at clinicaltrials.gov (NCT03647774).

Indexed as

NaltrexoneNarcotic AntagonistsOpioid-Related DisordersAdolescentAdultAgedDelayed-Action PreparationsFemaleHumansMaleMiddle AgedNorwayOpiate Substitution TreatmentRetrospective StudiesYoung AdultDelayed-Action PreparationsNaltrexoneNarcotic AntagonistsExtended-release naltrexoneMedically managed withdrawalOpioid use disorderTreatment induction

Identifiers

PMID40524244
PMCPMC12168299

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.