Laboratory Studies on Oxytocin for Treatment of Alcohol Use Disorder

Alcoholism Clinical Trial

Official title:

Laboratory Studies on Oxytocin for Treatment of Alcohol Use Disorder

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02407340
• Other study ID #: IRB00033324
• Status: Completed
• Phase: Phase 1
• First received: March 30, 2015
• Last updated: November 30, 2017
• Start date: March 2015
• Est. completion date: June 15, 2017

Study information

• Verified date: November 2017
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will examine the utility of the neuropeptide oxytocin (OT) as a potential new medication for the treatment of Alcohol use disorder (AUD). Non-treatment seeking men and women with AUD will be enrolled in a double blind placebo controlled phase I clinical trial. Participants will complete an 7-day inpatient protocol. During the first 3 days of the inpatient protocol, participants will complete alcohol abstinence in which withdrawal symptoms are measured,and urine will be collected to determine withdrawal symptom severity and urine levels of the stress hormone cortisol. Participants will then complete 3 laboratory procedures which measure 1) stress response, 2) motivation to drink alcohol and 3) subjective and physiological effects of alcohol. Finally, because participants are individuals with AUD, investigators will administer a brief intervention to address their risky alcohol drinking and problems before discharge.

Description:

This study will lay the necessary groundwork for future comprehensive research to examine the utility of the neuropeptide oxytocin (OT) as a potential new medication for the treatment of Alcohol use disorder (AUD). OT modulates a number of key systems involved in addiction processes, including dopamine (DA) mesolimbic reward circuitry, and hypothalamic-pituitary-adrenal (HPA) axis and corticotrophin-releasing factor (CRF) stress systems, and has low abuse liability. Our overarching hypothesis is that OT will attenuate several measures thought to drive compulsive alcohol drinking and relapse. Specifically, investigators will examine whether OT decreases acute stress responses, alleviates alcohol withdrawal symptoms, reduces craving and motivation to drink, and decreases alcohol self-administration. Since interactions with alcohol are an important focus of our study, investigators will enroll non-treatment seeking heavy drinkers with AUD in a double blind, placebo controlled inpatient protocol. Subjects will be randomized to receive intranasal OT (40 IU/dose) or placebo 3 times daily. Participants will complete alcohol detoxification; investigators will measure alcohol withdrawal symptoms, craving, and 24-hr urinary free CORT. Participants will then complete 3 laboratory procedures in fixed order. The Trier Social Stress Test (TSST) which includes public speaking and performance of mental arithmetic will be used to examine subjective and physiological stress responses. An alcohol motivated responding (AMR) procedure will be used to examine subjects' responding to earn either drinks or money. A cumulative alcohol-dosing (CAD) procedure will be used to examine physiological and subjective responses across several blood alcohol levels. cortisol (CORT) levels will also be assessed. This study will provide new information on OT efficacy across a range of different measures predictive of alcohol use and misuse, and, if OT shows efficacy, help clarify the mechanism of OT action.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 27
• Est. completion date: June 15, 2017
• Est. primary completion date: June 15, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years to 50 Years

Eligibility

Inclusion Criteria:

• Healthy 21-50 years old male and female subjects

• Must meet Diagnostic and Statistical Manual (DSM) -V criteria for AUD and not be seeking treatment

• Actively drinking

• Positive blood phosphatidylethanol (PEth) blood test

Exclusion Criteria:

• Current DSM-V major current mood or anxiety disorder or drug use disorder (excluding alcohol and nicotine use disorders, and moderate-severe cannabis use disorder); in or in need of treatment

• Drug use in last 30 days and/or positive urine toxicology screens (excluding marijuana)

• History of seizure disorder or closed head trauma

• History of withdrawal-related seizures or serious alcohol withdrawal symptoms

• HIV positive

• Neuroendocrine disorder

• Any serious medical condition that would place subject at risk or interfere with study participation

• Liver function tests more than 3 times normal at screening

• Prescription medications in last 3 months that could affect central nervous system or HPA axis function

• Women who are pregnant, nursing or planning pregnancy cannot participate

Related Conditions & MeSH terms

• Alcohol Related Disorders
• Alcohol-Related Disorders
• Alcoholism
• Disease

Intervention

Drug:
• oxytocin
40 international Units (IU) 3xday delivered as 5 sprays (0.1 mL) per nostril
• placebo
5 sprays (0.1 mL) per nostril 3xday; bottles are identical to those of active drug

Locations

Country	Name	City	State
United States	Johns Hopkins University	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
Johns Hopkins University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Alcohol drinking	Group mean number of Standard Drink Units earned and self-administered in the laboratory session	1 day
Secondary	alcohol effects	Group mean stimulation and sedation subscale scores on the biphasic alcohol effects scale (BAES), a 14-item scale consisting of adjectives that describe the stimulant- and sedative-like effects of alcohol. The items are presented in alphabetical order, and are rated on an 11-point rating scale from 0=Not at All to 10=Extremely after controlled alcohol administration.	1 day
Secondary	side effects	side effects reported on the Systematic Assessment for Treatment Emergent Events (SAFTEE)	1 week
Secondary	Salivary cortisol	Peak and Area under the curve salivary cortisol levels after trier social stress test	1 day