Brown University
Providence, Rhode Island, 02903, United States
Location status: Recruiting
Location contact
Brian Gully
CONTACT
Zoe Brown
CONTACT
NCT Number: NCT05988632
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.
Interested in participating?
Request Info21 year and older
All sexes
Interventional
Phase 1 / Phase 2
Providence, Rhode Island, 02903, United States
Location status: Recruiting
Brian Gully
CONTACT
Zoe Brown
CONTACT
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Insulin: 80 IU (administered intranasally) THEN Placebo: 0.9% saline solution (administered intranasally)
Other names: Novolin R
Placebo: 0.9% saline solution (administered intranasally) THEN Insulin: 80 IU (administered intranasally)
Other names: Novolin R
Time frame: From baseline to post-treatment (1 day)
Adverse event reported during the drug administration
Time frame: From baseline to post-treatment (1 day)
Adverse event reported during the alcohol administration
Contact information is provided by the study sponsor or research team.
Brown University
Other
Acronym: ITA
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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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