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NCT Number: NCT05988632

Intranasal Insulin for Treatment of Alcohol Use Disorder

This is a randomized controlled trial (RCT), within-subject, crossover, double-blind, placebo-controlled in non-treatment-seeking individuals with Alcohol Use Disorder (AUD) (N=40, 50% female) randomized to IN insulin or placebo. In a bar laboratory setting, randomized participants will receive a single dose of IN insulin (80IU) or an IN matched placebo (0.9% Saline). Participants will undergo a cue-reactivity paradigm followed by an alcohol challenge that includes an alcohol drink designed to raise the breath alcohol content (BrAC) to 0.08g/dL.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

About this study

Aims in this RCT testing the effect of IN insulin, compared to placebo, in individuals with AUD include the following:

AIM 1: to assess the safety, tolerability and acceptability of IN insulin as a pharmacological intervention for AUD. The data collected in this aim will monitor possible adverse events and yield qualitative and quantitative data to finalize the feasibility and acceptability of IN insulin as an AUD pharmacotherapy.

Aim 2 (alcohol-drug interaction): to assess the safety and tolerability of IN insulin when administered with alcohol. The investigators will use a battery of physiological/psychological assessments that measures potential adverse events, alcohol subjective response and alcohol pharmacokinetics endpoints.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ≥21 years
  • meet any DSM-5 criteria score for AUD
  • Individuals who, in the last month, have consumed at least the same amount of alcohol that will be administered in the laboratory procedure (i.e. to reach BrAC levels of 0.08g/dl, ~two drinks in one occasion)
  • BrAC=0.00g/dL at each visit
  • good health as confirmed by medical history, physical examination and lab tests
  • willing to adhere to the study procedures
  • understand informed consent and questionnaires in English at an 8th grade level
  • willing to have glucose monitored by finger stick during the laboratory procedures

Exclusion criteria

  • • female identifying who are breastfeeding or pregnant (assessed by a urine screen)
  • individuals with diabetes
  • history of suicide attempts in the last three years
  • current diagnosis of other substance use disorder (other than nicotine or cannabis)
  • use of drugs (e.g. stimulants/opioids) at each alcohol administration session (by urine tox screen)
  • cannabis intoxication (by clinical assessments)
  • use of medications that may interact with insulin and alcohol (by Micromedex database)
  • hypersensitivity to insulin
  • any nasal disease/congestion that may interfere with intranasal drug absorption;
  • baseline hypoglycemia (blood glucose ≤65mg/dL) or hyperglycemia (blood glucose >200mg/dL) (by finger stick)

Treatment and study plan

Regular Human Insulin then Placebo

Drug

Insulin: 80 IU (administered intranasally) THEN Placebo: 0.9% saline solution (administered intranasally)

Other names: Novolin R

Placebo then Regular Human Insulin

Drug

Placebo: 0.9% saline solution (administered intranasally) THEN Insulin: 80 IU (administered intranasally)

Other names: Novolin R

Primary outcomes

  1. intranasal adverse events

    Time frame: From baseline to post-treatment (1 day)

    Adverse event reported during the drug administration

Secondary outcomes

  1. insulin alcohol interaction

    Time frame: From baseline to post-treatment (1 day)

    Adverse event reported during the alcohol administration

Study contacts

Contact information is provided by the study sponsor or research team.

Carolina L Haass-Koffler

CONTACT

[email protected]

4155191385

Sponsors and collaborators

Lead sponsor

Brown University

Other

Registry information

Acronym: ITA

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Aug 14, 2023
Registry last updated
Sep 5, 2025

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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