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OpenTrials
Completed

NCT Number: NCT01394757

Network Dysfunction, Schizophrenia and Pharmacological Magnetic Resonance Imaging (phMRI)

Alterations of functional brain networks have been frequently demonstrated in schizophrenia, although the exact underlying molecular mechanisms remain unrevealed. Ketamine is known to exert its schizophrenia-like effects through modulation of the glutamatergic system, thus facilitating the investigation of the impact of this specific transmitter system on resting state functional brain networks. The aim of the study is therefore to use pharmacological functional Magnetic Resonance Imaging (phMRI) to examine changes in brain networks involved in schizophrenia in response to ketamine application compared to placebo. 30 healthy subjects (15 females) will be examined twice using a double-blind, placebo-controlled, randomized, crossover, counterbalanced-order design. Resting state fMRI will be investigated before, during and after either placebo or ketamine intravenous infusion for 20 minutes. Prior to the main trial 10 additional participants will be included in an open pilot trial.

Hypothesis: Ketamine application will induce changes in resting state networks previously associated with schizophrenia and in the connectivity of relevant brain regions such as the striatum, thalamus, caudate, hippocampus and amygdala. Furthermore, the application of ketamine will provoke changes in the BOLD-activation in three fMRI paradigms each performed before and after ketamine infusion.

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Key information

Conditions

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Psychiatry and Psychotherapy, Medical University of Vienna

Vienna, State of Vienna, 1090, Austria

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • general health based on history, physical examination, ECG, laboratory screening and structured clinical interview for DSM-IV(SCID)
  • willingness and competence to sign the informed consent form
  • aged 18 to 55 years

Exclusion criteria

  • any medical, psychiatric or neurological illness
  • current or former substance abuse
  • any implant or stainless steel graft and any other contraindications for MRI
  • pregnancy
  • first degree relatives with a history of psychiatric illness or substance abuse
  • failures to comply with the study protocol or to follow the instructions of the investigating team
  • lifetime use of antipsychotic drugs
  • treatment with psychotropic agents such as SSRIs within the last 6 months

Treatment and study plan

Esketamine hydrochloride

Drug

Bolus: 15 mg/kg over 1 minute, followed by a maintenance infusion of 0.25 mg/kg/h for 19 minutes.

Other names: Ketanest S, Ketamine

Primary outcomes

  1. Ketamine-induced changes in BOLD-activity over time

    Time frame: 1 year

    participants will be measured twice and all participants are expected to be recruited and measured within 1 year

Secondary outcomes

  1. Change of task-induced BOLD-activity by ketamine application

    Time frame: 60 minutes (before and after ketamine infusion) at each MRI session (interval between MRI scans: 1 week)

Sponsors and collaborators

Lead sponsor

Medical University of Vienna

Other

Registry information

Official study title

Brain Network Dysfunction as a Model for Schizophrenia: Connectivity Alterations Using Ketamine and Pharmacological Magnetic Resonance Imaging

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Jul 14, 2011
Registry last updated
Dec 31, 2013

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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