Brown University
Providence, Rhode Island, 20923, United States
NCT Number: NCT04135846
The goal of this research is to replicate findings previously conducted in a pilot trial and to understand, mechanistically, the role of stress in the development of AUD pharmacotherapies that target noradrenergic blockade.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Phase 2
Providence, Rhode Island, 20923, United States
16 week, between-subject, double-blind, randomized clinical trial (RCT) with doxazosin (16 mg, or maximum tolerated dose, MTD) compared to placebo in 184 treatment seeking individuals with AUD
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
16 mg or maximum tolerated dose (MTD)
Other names: Cardura
Matching placebo
Time frame: 6 weeks
Number of drinks per week (DPW) in naturalistic condition as measured by the timeline follow-back (TLFB)
Time frame: one day
We will measure alcohol craving using the Alcohol Craving Questionnaire (ACQ) after a cue-reactivity
Time frame: six weeks
Alcohol craving in naturalistic condition will be measured using craving the Obsessive Compulsive Drinking Scale (OCDS)
This study is active but is not currently recruiting participants.
Notify MeBrown University
Other
A Focus on Alpha-1 Blockade as a Novel Pharmacological Treatment for AUD
Acronym: DOXY
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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