CompletedPhase 1ketamine

The Effect of Ketamine on Attentiveness

Sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

NCT ID
NCT01165294
Target Enrollment
24 participants
Start Date
2009-10
Est. Completion
2010-05

About This Study

The objective of this study is to develop an exploratory design for future Proof-of-Concept trials which reliably and accurately measure the central nervous system (CNS) effects of potentially new drugs that oppose the effects of ketamine at a subanesthetic dose level given to healthy volunteers. A functional magnetic resonance imaging (fMRI) and electroencephalogram (EEG) performed simultaneously during a ketamine challenge will register the effects triggered by Ketamine.

Conditions Studied

Schizophrenia

Interventions

  • Placebo
  • ketamine

Eligibility

Age:18 Years - 35 Years
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* Normal ECG and safety assessments, or minor no-relevant deviations, at screening
* Vital signs: systolic between 100 and 140 mmHg and diastolic between 50 and 90 mmHg and heart rate between 45 and 90 beats/min
* No medication intake in the last four weeks
* Volunteers must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study and to adhere to the prohibitions and restrictions specified in the protocol
* Negative drug screen

Exclusion Criteria:

* Participation in another clinical trial in the last 3 months
* Significant allergies, allergic diathesis or known hypersensitivity for ketamine or its ingredients (ie, Benzethonium chloride)
* History of or current significant respiratory disease, cardiovascular disease, endocrinological, gastrointestinal, neurological, glaucoma and known liver and kidney failure
* Contraindications for an MRI being performed (claustrophobia, metal parts, pacemaker)
* oxygen saturation pO2 \< 90 mmHg
* Clinically significant abnormalities in ECG or laboratory values
* Recent history (within previous 6 months) of alcohol or drug abuse
* History of or current psychiatric diagnoses (DSM-IV, II) or neurological disorders
* Relatives in first or second degree with a schizophrenic disorder
* Serology positive for hepatitis B surface antigen, hepatitis C antibodies or HIV antibodies
* Signs of hyperthyroidism based on the determination of T3, T4 and TSH

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source