Informazioni generali
  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Zurigo
    (BASEC)
  • Responsabile dello studio Patricia Dürler patricia.duerler@bli.uzh.ch (BASEC)
  • Fonte dati BASEC: Importato da 11.04.2025 ICTRP: N/A
  • Ultimo aggiornamento 11.04.2025 12:00
HumRes66674 | SNCTP000006363 | BASEC2024-02294

Investigation of the Combined Effect of Ketamine and Neurofeedback Training in the Treatment of Alcohol Use Disorder

  • Categoria della malattia Altro (BASEC)
  • Stato di reclutamento reclutamento non ancora iniziato (BASEC/ICTRP)
  • Luogo dello studio
    Zurigo
    (BASEC)
  • Responsabile dello studio Patricia Dürler patricia.duerler@bli.uzh.ch (BASEC)
  • Fonte dati BASEC: Importato da 11.04.2025 ICTRP: N/A
  • Ultimo aggiornamento 11.04.2025 12:00

Descrizione riassuntiva dello studio

In this study, we investigate the effects of combining ketamine and neurofeedback training for the treatment of alcohol use disorder. Participants will be randomly assigned – like a coin toss – to one of three groups: ketamine with neurofeedback, placebo (an inactive substance) with neurofeedback, or ketamine with 'sham' neurofeedback (which provides no real feedback). Neither the participants nor the researchers will know which treatment they receive, ensuring unbiased results. The goal is to examine whether ketamine and neurofeedback, individually or in combination, can help reduce alcohol cravings and support treatment.

(BASEC)

Intervento studiato

This clinical study aims to investigate the effects of combining ketamine infusions with neurofeedback training for the treatment of alcohol use disorder. Participants will be randomly assigned to one of three groups, each undergoing a specific investigation that is part of the clinical study. The groups and their respective interventions are as follows:

1. Ketamine + Neurofeedback Training

Participants in this group will receive an intravenous infusion of ketamine at a dose of 0.8 mg/kg, administered over approximately 40 minutes. After the infusion, they will participate in neurofeedback training sessions. These sessions target specific brain regions associated with alcohol cravings and self-regulation, helping participants gain better control over their responses to alcohol-related triggers. The neurofeedback training sessions (each lasting 25 minutes) will take place on two different days, aiming to examine whether the combination of ketamine and neurofeedback training reduces alcohol cravings more effectively than other approaches.

2. Placebo + Neurofeedback Training

This group will receive an intravenous infusion of a placebo (saline solution), administered over approximately 40 minutes, mimicking the experience of ketamine administration without the active ingredient. Subsequently, participants will engage in the same neurofeedback training as the ketamine + neurofeedback group. This group serves as a control group to investigate the influence of neurofeedback training alone on reducing alcohol use disorder symptoms.

3. Ketamine + Sham Neurofeedback

In this group, participants will receive ketamine at the same dose (0.8 mg/kg) and duration as in the ketamine + neurofeedback group. Instead of real neurofeedback training, they will participate in sham neurofeedback training, where they receive feedback that does not reflect their actual brain activity. This approach allows researchers to examine the effects of ketamine independently of active neurofeedback training and determine whether ketamine alone has an impact on outcomes related to alcohol use disorder.

These three interventions will help us investigate the individual and combined effects of ketamine and neurofeedback training on reducing alcohol cravings and supporting the long-term treatment of alcohol use disorder.

(BASEC)

Malattie studiate

Alcohol Use Disorder

(BASEC)

Criteri di partecipazione
• DSM-IV diagnosis of alcohol use disorder (mild to severe) • Motivation to reduce or stop alcohol consumption • Good physical health without unstable medical conditions (BASEC)

Criteri di esclusione
• History of severe substance use disorder according to DSM-IV (except alcohol, excluding caffeine or nicotine) within two months prior to participation, as well as any opioid use disorder within two months prior to participation. • Life history of bipolar disorder or schizophrenia/schizoaffective disorder/psychosis (BASEC)

Luogo dello studio

Zurigo

(BASEC)

non disponibile

Sponsor

Dr. Marcus Herdener

(BASEC)

Contatto per ulteriori informazioni sullo studio

Persona di contatto in Svizzera

Patricia Dürler

+41583843324

patricia.duerler@bli.uzh.ch

University of Zurich

(BASEC)

Informazioni scientifiche

non disponibile

Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)

Commissione etica Zurigo

(BASEC)

Data di approvazione del comitato etico

11.04.2025

(BASEC)


ID di studio ICTRP
non disponibile

Titolo ufficiale (approvato dal comitato etico)
Phase II, randomised, placebo-controlled, double blind, parallel group, single centre study investigating ketamine and neurofeedback as combined therapeutic interventions to target glutamatergic neurotransmission in alcohol use disorder. (BASEC)

Titolo accademico
non disponibile

Titolo pubblico
non disponibile

Malattie studiate
non disponibile

Intervento studiato
non disponibile

Tipo di studio
non disponibile

Disegno dello studio
non disponibile

Criteri di inclusione/esclusione
non disponibile

non disponibile

Endpoint primari e secondari
non disponibile

non disponibile

Data di registrazione
non disponibile

Inclusione del primo partecipante
non disponibile

Sponsor secondari
non disponibile

Contatti aggiuntivi
non disponibile

ID secondari
non disponibile

Risultati-Dati individuali dei partecipanti
non disponibile

Ulteriori informazioni sullo studio
non disponibile

Risultati dello studio

Riepilogo dei risultati

non disponibile

Link ai risultati nel registro primario

non disponibile