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Citicoline in Youth Alcohol Use Disorder

Medical University of South Carolina (MUSC) logo

Medical University of South Carolina (MUSC)

Status and phase

Enrolling
Phase 2

Conditions

Alcohol Use Disorder

Treatments

Drug: Citicoline (cytidine diphosphate-choline)
Drug: Placebo oral capsule

Study type

Interventional

Funder types

Other

Identifiers

NCT05870111
Pro00128800

Details and patient eligibility

About

The goal of this study is to evaluate how citicoline, an over-the-counter supplement, versus a placebo pill (i.e., an inactive pill) affects the immune system, brain, and cognition in adolescents who may use alcohol.

Enrollment

56 estimated patients

Sex

All

Ages

16 to 22 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

Age 16 to 22.

Call study team for additional screening and information.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

56 participants in 2 patient groups, including a placebo group

Citicoline
Experimental group
Description:
2000mg/day citicoline for 4 weeks, administered orally
Treatment:
Drug: Citicoline (cytidine diphosphate-choline)
Placebo
Placebo Comparator group
Description:
placebo capsule daily for 4 weeks, matched in appearance to citicoline to preserve double-blind, administered orally
Treatment:
Drug: Placebo oral capsule

Trial contacts and locations

1

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Central trial contact

Cori Herring, BS

Data sourced from clinicaltrials.gov

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