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Completed

NCT Number: NCT05093296

Oxytocin and Naltrexone: Investigation of Combined Effects on Stress- and Alcohol Cue-induced Craving in Alcohol Use Disorder

Alcohol use disorder (AUD) is a chronic relapsing disorder. Alcohol craving, a hallmark symptom of AUD that drives relapse in patients, is only insufficiently treated by existing medication. One promising new compound is Oxytocin (OXY), which showed beneficial effects on alcohol craving in preliminary clinical studies. Additionally, OXY seems to enhance effects of established medication, specifically Naltrexone (NTX), an opioid-antagonist which is approved for AUD treatment via positive synergism on neurotransmitter levels. The proposed two-armed, 1:1 randomized, double-blind, parallel group trial seeks to test the putative synergistic effects of combined intranasal OXY spray (24 IU) + oral NTX (50mg) against Placebo spray + oral NTX (50mg) on alcohol craving (primary outcome) in male and female patients with AUD that suffer from high alcohol craving, within the framework of a validated alcohol cue-and stress-exposure task (i.e. a combined Trier Stress Test and alcohol cue-exposure) that was established for screening new medications in AUD and determine their effects on craving and relapse risk. Treatment effects on additional neurobiological and biochemical markers of craving that show strong associations to individual relapse risk, will serve as secondary outcomes. Collection and analysis of follow-up data (90 days) will be performed to determine whether treatment effects relate to patient outcome.

The clinical trial period for an individual participant consists of a screening visit (visit 1), a baseline visit (visit 2) and two treatment visits (visits 3 and 4)(all within equal or less than ten days) followed by a 90 days (+/- 7 days) follow-up phase with two visits (visits 5 and 6) at day 30 (± 7 days) and day 90 (± 7 days). Visits 1 to 4 will be conducted while participants are undergoing standard in-patient treatment at the Department of Addictive Behavior and Addiction medicine at the Central Institute of Mental Health (CIMH) in Mannheim, Germany, for the medical condition under investigation.

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Key information

Conditions

Alcohol Use Disorder Alcohol Addiction Alcohol-Related Disorders Alcoholism Chemically-Induced Disorders Mental Disorders Substance-Related Disorders

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Central Institute of Mental Health

Mannheim, 68159, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 18 and 70 years
  • Patients meeting the diagnosis of an alcohol dependence according to the Internation Clasification of Diseases 10th revision (ICD10)
  • Patients with at least moderate craving, i.e. either >=15 points on the Alcohol Urge Questionnaire (AUQ, range 8 to 56 points) craving scale or increase in AUQ scores by >= 50% after exposure to visual alcohol cues (i.e. minimum increase of >=4 points after cue exposure)
  • Ability of the individual to understand the character and the individual consequences of the clinical trial
  • Written informed consent (must be available before enrollment in the study)
  • Consent to random assignment
  • For women with childbearing potential, use of a highly effective birth control method until 24 hours after Visit 4 and negative pregnancy test

Exclusion criteria

  • Subjects presenting with any of the following criteria will not be included in the clinical trial: Current psychotic or bipolar disorder or current severe depressive episode with suicidal ideations
  • Current treatment with any of the following substances: Any investigational medicinal product, Opioid-containing Analgesics, Anorexics, Anticonvulsants, Opioid-containing Antidiarrheal Agents, Antineoplastics, Antipsychotics (exception: episodic use of melperone, pipamperone and quetiapine are allowed), Antidepressants (exception: allowed, when being taken in stable dose for a minimum of 14 days prior to enrolment and/or doxepin in low doses [max. 75mg daily]), Opioid-containing Cough/cold agents, systemic Steroids
  • Positive drug screening (amphetamines/ecstasy, opiates, cocaine, barbiturates)
  • Pregnancy, lactation or breastfeeding
  • Current severe somatic comorbidities: liver cirrhosis [CHILD B or C] or impaired renal function [glomerular filtration rate (GFR)<15ml/Min] [each determined by physical examination and/or laboratory testing], severe heart insufficiency [determined by assessment of medical history], pre-existing epilepsy [determined by assessment of medical history], long-QT syndrome or cardial arrhythmia [determined by ECG]
  • History of hypersensitivity to the investigational medicinal product Oxytocin (Syntocinon®) and/or Naltrexone (trade names: Adepend, Naltrexon-Hcl neuraxpharm, Naltrexonhydrochlorid Accord) or to any drug with similar chemical structure or to any excipient present in the pharmaceutical form of the investigational medicinal product Oxytocin (Syntocinon®) and/or Naltrexone
  • Participation in other clinical trials or observation period of competing clinical trials, respectively.
  • Acute suicidal tendency or acute endangerment of self and others

Treatment and study plan

Oxytocin nasal spray

Drug

24 I.U. Oxytocin nasal Spray will be administered twice on two separate trial days.

Naltrexone Pill

Drug

All participants will receive 50mg Naltrexone daily as oral tablet throughout the study

Placebo

Drug

Placebo nasal spray (same composition as the verum oxytocin spray except for the active ingredient oxytocin)

Primary outcomes

  1. Alcohol Urge Questionnaire (AUQ)

    Time frame: 60 minutes after oxytocin/placebo application and directly after the combined stress- and cue-exposure will serve as primary outcome measure at Visit 3

    Subjective Alcohol Craving will be assessed at separate time points before and after Oxytocin Administration using the AUQ

Secondary outcomes

  1. Alcohol Urge Questionnaire (AUQ)

    Time frame: 35 minutes after oxytocin/placebo application at Visit 3

    Subjective Alcohol Craving will be assessed at separate time points before and after Oxytocin Administration using the AUQ

  2. Alcohol Urge Questionnaire (AUQ)

    Time frame: 70 minutes after oxytocin/placebo application at Visit 3

    Subjective Alcohol Craving will be assessed at separate time points before and after Oxytocin Administration using the AUQ

  3. Alcohol Urge Questionnaire (AUQ)

    Time frame: 80 minutes after oxytocin/placebo application at Visit 3

    Subjective Alcohol Craving will be assessed at separate time points before and after Oxytocin Administration using the AUQ

  4. Alcohol Urge Questionnaire (AUQ)

    Time frame: 90 minutes after oxytocin/placebo application at Visit 3

    Subjective Alcohol Craving will be assessed at separate time points before and after Oxytocin Administration using the AUQ

  5. Alcohol Urge Questionnaire (AUQ)

    Time frame: 85 minutes after oxytocin/placebo application, i.e. directly fMRI session at Visit 4

    Subjective Alcohol Craving will be assessed at separate time points before and after Oxytocin Administration using the AUQ

  6. Primary Appraisal secondary Appraisal Scale (PASA)

    Time frame: 35 minutes after oxytocin/placebo application at Visit 3

    Perceived stress will be assessed using the Primary Appraisal secondary Appraisal Scale (PASA) at separate time points before and after Oxytocin Administration using the AUQ at Visit 3 and Visit 4

  7. Primary Appraisal secondary Appraisal Scale (PASA)

    Time frame: 60 minutes after oxytocin/placebo application at Visit 3

    Perceived stress will be assessed using the Primary Appraisal secondary Appraisal Scale (PASA) at separate time points before and after Oxytocin Administration using the AUQ at Visit 3 and Visit 4

  8. Primary Appraisal secondary Appraisal Scale (PASA)

    Time frame: 90 minutes after oxytocin/placebo application at Visit 3

    Perceived stress will be assessed using the Primary Appraisal secondary Appraisal Scale (PASA) at separate time points before and after Oxytocin Administration using the AUQ at Visit 3 and Visit 4

  9. Primary Appraisal secondary Appraisal Scale (PASA)

    Time frame: 85 minutes after oxytocin/placebo application, i.e. directly fMRI session at Visit 4

    Perceived stress will be assessed using the Primary Appraisal secondary Appraisal Scale (PASA) at separate time points before and after Oxytocin Administration using the AUQ at Visit 3 and Visit 4

  10. Positive and Negative Affect Schedule (PANAS)

    Time frame: 60 minutes after oxytocin/placebo application at Visit 3

    Positive and Negative Affect will be assessed using the Positive and Negative Affect Schedule (PANAS) at separate time points before and after Oxytocin Administration using the AUQ at Visit 3 and Visit 4

  11. Positive and Negative Affect Schedule (PANAS)

    Time frame: 85 minutes after oxytocin/placebo application, i.e. directly fMRI session at Visit 4

    Positive and Negative Affect will be assessed using the Positive and Negative Affect Schedule (PANAS) at separate time points before and after Oxytocin Administration using the AUQ at Visit 3 and Visit 4

  12. Cortisol

    Time frame: 65 minutes after oxytocin/placebo application at Visit 3

    Cortisol plasma levels will be determined using validated Enzyme-linked Immunosorbent Assay (ELISA) methods by the central laboratory at visit 3 after Oxytocin/Placebo administration

  13. Oxytocin

    Time frame: 30 minutes after oxytocin/placebo application at Visit 3

    Oxytocin plasma levels will be determined using validated ELISA methods by the central laboratory at visit 3 after Oxytocin/Placebo administration

  14. Oxytocin

    Time frame: 65 minutes after oxytocin/placebo application at Visit 3

    Oxytocin plasma levels will be determined using validated ELISA methods by the central laboratory at visit 3 after Oxytocin/Placebo administration

  15. Alcohol Cue-induced neural brain activation during an Alcohol cue-reactivity functional magnetic resonance imaging (fMRI) task

    Time frame: During fMRI session at Visit 4, i.e. 40 to 85 minutes after Oxytocin/Placebo administration

    Neural brain activation in the mesocorticolimbic system (whole-brain and Region-of-Interest Analyses (ROIs): ventral striatum, dorsal striatum, insula), measured using the blood oxygenated level dependent (BOLD) response, during presentation of alcohol cues will serve as secondary outcome

  16. Neural Activation during a natural reward cue-reactivity fMRI task

    Time frame: During fMRI session at Visit 4, i.e. 40 to 85 minutes after Oxytocin/Placebo administration

    Neural brain activation in the mesocorticolimbic system (whole-brain and ROIs: ventral striatum, dorsal striatum, insula), measured using the blood oxygenated level dependent (BOLD) response during the presentation of natural reward cues will serve as secondary outcome

  17. Neural Activation during a Face-matching fMRI task

    Time frame: During fMRI session at Visit 4, i.e. 40 to 85 minutes after Oxytocin/Placebo administration

    Neural brain activation in the mesocorticolimbic system (whole-brain and ROIs: ventral striatum, dorsal striatum, insula, amygdala), measured using the blood oxygenated level dependent (BOLD) response during the presentation of emotional faces and neutral shapes will serve as secondary outcome

  18. Neural Activation during a Stop Signal fMRI Task

    Time frame: During fMRI session at Visit 4, i.e. 40 to 85 minutes after Oxytocin/Placebo administration

    Neural brain activation in the mesocorticolimbic system (whole-brain and ROIs: ventral striatum, dorsal striatum, insula, dlPFC), measured using the blood oxygenated level dependent (BOLD) response during a stop signal fMRI task will serve as secondary outcome

  19. Adverse Events (AEs)/Serious Adverse Events (SAEs) and Discontinuation rate

    Time frame: During Study Visits 1 to 6, including the 90 day (±7 day) follow-up period

    Rate of adverse events, serious adverse events and rate of discontinuation of the study due to an adverse event

  20. Subjective quality of life index

    Time frame: At Visit 5, i.e. 30 days (+/- 7 days) after Visit 3

    Quality of life will be assessed using the WHO-QOL-BREF scores

  21. Subjective quality of life index

    Time frame: At Visit 6, i.e. 90 days (+/- 7 days) after Visit 3

    Quality of life will be assessed using the World Health Organization (WHO) Quality of life assessment (WHO-QOL-BREF) scores

  22. Time to relapse during the follow-up period of 90 days (+/- 7 days)

    Time frame: During 90-day (± 7 days) Follow-up

    Time from randomization to relapse to alcohol use (in days)

  23. Cumulative alcohol consumption during the follow-up period of 90 days (+/- 7 days)

    Time frame: During 90-day (± 7 days) Follow-up

    Self-reported cumulative alcohol use (in gram)

  24. Percent heavy drinking days during the follow-up period of 90 days (+/- 7 days)

    Time frame: During 90-day (± 7 days) Follow-up

    Self-reported percent heavy drinking days (in %)

Sponsors and collaborators

Lead sponsor

Central Institute of Mental Health, Mannheim

Other

Collaborators

  • German Federal Ministry of Education and Research
  • Heidelberg University
  • Heinrich-Heine University, Duesseldorf

Registry information

Official study title

Oxytocin and Naltrexone: Investigation of Combined Effects on Stress- and Alcohol Cue-induced Craving in Alcohol Use Disorder - a Randomized Double-blind Placebo-controlled Parallel-group Trial

Acronym: ON-ICE

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Oct 26, 2021
Registry last updated
Mar 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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