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Trial of transcranial direct current stimulation (tDCS) on craving in alcohol Users

Randomized, single blind, controlled trial of transcranial direct current stimulation (tDCS) on craving in Alcohol Use Disorder

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039412
Enrollment
30
Registered
2022-01-13
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F102- Alcohol dependence

Interventions

Intervention1: Transcranial direct current stimulation: Total number of 5 sessions over a period of 1 week will be given, each session of 20 minutes. Anode will be placed over Right DLPFC and cathod

Sponsors

King George medical university
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between 18 and 60 years Informed consent for participation in the study from the patient diagnosed with Alcohol Use Disorder (Using DSM-5 [The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition] criteria) Clinical Institute Withdrawal Assessment for Alcohol Scale, Revised (CIWA AR score) Alcohol Urge Questionnaire Score >24

Exclusion criteria

Exclusion criteria: Any other psychiatric disorder (except tobacco use disorder) Clinically assessed Intellectual disability Intoxicated state or history of complicated withdrawal, seizure or delirium tremens in currrent episode Any significant medical comorbidity Any contraindication for electrical brain stimulation procedures

Design outcomes

Primary

MeasureTime frame
To study the efficacy of Transcranial Direct Current Stimulation on craving in patients with Alcohol Use Disorder.Timepoint: follow up in 1, 4 and 8 weeks

Secondary

MeasureTime frame
To study the safety of Transcranial Direct Current Stimulation on craving in patients with Alcohol Use Disorder. To study the feeling of well-being in patients of Alcohol Use Disorder Timepoint: follow up in 1, 4 and 8 weeks

Countries

India

Contacts

Public ContactArundhati Gairola

King Georges Medical University UP Lucknow

an.kgmu@gmail.com9935719000

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026