Clinical trial

The Neural Mechanisms Associated With Alcohol and Cigarette Craving in Alcohol Use Disorder Smokers During Oxytocin Treatment

Name
22301
Description
This proposed research seeks to examine the behavioral and neural substrates of intranasal oxytocin compared to placebo on alcohol cue-induced alcohol and cigarette craving smokers with an alcohol use disorder (AUD). Non treatment-seeking smokers with an AUD will be recruited to participate in a between-subjects, placebo-controlled, randomized pilot functional magnetic resonance imaging (fMRI) study. Participants will undergo an fMRI scan in conjunction with an alcohol-olfactory cue-reactivity task. Secondary assessments will include alcohol and cigarette craving, alcohol and cigarette consumption, physiological measures (heart rate and blood pressure) and mood measures.
Trial arms
Trial start
2020-11-09
Estimated PCD
2024-04-02
Trial end
2024-04-02
Status
Completed
Phase
Early phase I
Treatment
Oxytocin nasal spray
Participants administer the oxytocin (40 IU) twice a day for 5 - 7 days
Arms:
Oxytocin nasal spray
Placebo
Participants administer the placebo (40 IU) twice a day for 5 - 7 days
Arms:
Placebo
Size
19
Primary endpoint
Alcohol craving
1 day
Cigarette craving
1 day
Brain activity
1 day
Eligibility criteria
Inclusion Criteria: 1. male or female 2. 18 to 55 years of age 3. meet criteria for Alcohol Use Disorder DSM-5 diagnosis 4. meet the National Institute on Alcohol Abuse and Alcoholism criteria for heavy-drinking 5. smoke at least ≥5 cigarettes/day for at least a year, verified with breath carbon monoxide level \> 5 ppm 6. in good health as confirmed by medical history, physical examination and lab tests 7. willing to take the medication and adhere to the study procedures 8. breath alcohol concentration (BrAC) = 0.00 at each visit 9. understand informed consent and questionnaires written in English at an 8th grade level 10. right-handedness 11. normal to normal-corrected vision Exclusion Criteria: 1. positive urine test for pregnancy 2. women who are breast-feeding 3. body mass index \> 40 4. current or prior history of any clinically significant disease, cardiovascular, respiratory, gastrointestinal, hepatic, renal, endocrine, or reproductive disorders, positive hepatitis or HIV test that could affect study participation, as determined by the study physician 5. history of suicide attempts 6. current diagnosis of substance dependence other than alcohol, nicotine or cannabis as assessed by self-report and urine toxicology screen at baseline 7. current use of psychoactive medications or any medication that may interact with oxytocin 8. history of hypersensitivity to oxytocin 9. chronic rhinitis or sinusitis 10. clinically significant electrolyte abnormalities 11. vasoconstricting medications or prostaglandins 12. clinically significant medical abnormalities: unstable hypertension, bilirubin \>150% of the upper normal limit (UNL), ALT/AST \>500% the UNL, creatinine clearance ≤60 dl/min) 13. significant alcohol withdrawal symptoms, defined as a CIWA-Ar \> 8 14. positive urine drug screen at baseline for any excluded substances 15. individuals seeking treatment 16. meets DSM-5 criteria for a diagnosis of schizophrenia, bipolar disorder, or other psychoses 17. claustrophobia 18. any contraindications with the MRI machine
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'OTHER', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 19, 'type': 'ACTUAL'}}
Updated at
2024-05-14

1 organization

1 product

1 drug

2 indications

Organization
Brown University
Product
Oxytocin