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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03333369
Other study ID # DA_EE_Salience
Secondary ID
Status Completed
Phase Early Phase 1
First received October 30, 2017
Last updated November 2, 2017
Start date May 15, 2014
Est. completion date August 13, 2015

Study information

Verified date November 2017
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The dopamine hypothesis of schizophrenia implies that alterations in the dopamine system cause functional abnormalities in the brain that may converge to aberrant salience attribution and eventually lead to psychosis. Indeed, widespread brain disconnectivity across the psychotic spectrum has been revealed by resting-state functional magnetic resonance imaging (rs-fMRI). However, the dopaminergic involvement in intrinsic functional connectivity (iFC) and its putative relationship to the development of psychotic spectrum disorders remains partly unclear - in particular at the low-end of the psychosis continuum. Therefore, the investigators examined dopamine-induced changes in striatal iFC and their modulation by psychometrically assessed schizotypy. The randomized, double-blind placebo-controlled study design included 54 healthy, right-handed male participants. Each participant was assessed with the Schizotypal Personality Questionnaire (SPQ) and underwent 10 min of rs-fMRI scanning. Participants then received either a placebo or 200 mg of L-DOPA, a dopamine precursor. The investigators analyzed iFC of six striatal seeds that are known to evoke modulation of dopamine-related networks.

The investigators hypothesized that, within the L-DOPA treatment group, the striatal iFC would be disrupted due to increased availability of dopamine. The investigators further hypothesized that individuals with high schizotypal scores would show a disruption of striatal connectivity, as has been reported with schizophrenia. In addition, the investigators hypothesized that the L-DOPA-dependent change in striatal iFC would interact with the severity of positive symptoms, as has been found in previous studies in non-clinical psychosis. The investigators anticipated this symptom-dependent change, especially in the ventral striatal regions, because these are thought to modulate cortico-striatal loops associated with cognition and emotion.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date August 13, 2015
Est. primary completion date August 13, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Healthy,

- Between 20 and 40 years of age,

- With exceptional experiences or skeptics,

- Caucasian origin,

- Normal visual and acoustic accuracy.

Exclusion Criteria:

- Persons with a personal or first-degree family history of neurological and psychiatric disease, including impaired cognitive abilities,

- Pregnant or breastfeeding women,

- Chronic or acute pain,

- Acute or chronic somatic disease,

- Women (i.e. only men included),

- Men over 40 years of age or below 20,

- left- or mixed-handedness,

- General MRI exclusion criteria,

- General Dopamine-Challenge exclusion criteria,

- Hormonal or herbal therapy,

- Smoker.

Study Design


Intervention

Drug:
200 mg levodopa/50 mg benserazide

Dextrose


Locations

Country Name City State
Switzerland Collegium Helveticum, ETH & Universität Zürich Zürich

Sponsors (2)

Lead Sponsor Collaborator
University of Zurich Swiss Federal Institute of Technology

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary intrinsic functional connectivity Dopamine dependent intrinsic functional connectivity as measured by resting-state functional magnetic resonance imaging 2 hours
Secondary Schizotypy Schizotypy scores assessed by the Schizotypal Personality Questionnaire (SPQ):
n of items 74 (min. score = 0 ; max. score = 74): higher score implies higher level of schizotypy
Subscales:
Cognitive Perceptual (min. score = 0 ; max. score = 33)
Interpersonal (min. score = 0 ; max. score = 25)
Disorganized (min. score = 0 ; max. score = 16)
15 min
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