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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02511691
Other study ID # KEK ZH 2014-0441
Secondary ID
Status Terminated
Phase Phase 2
First received
Last updated
Start date July 2015
Est. completion date March 3, 2016

Study information

Verified date August 2020
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Based on PET (18-PSS232) and MRI, glutamate release after N-acetylcystein challenge will be monitored in human brains.


Description:

Diagnostic trial with quantification of glutamate release in PET/MR.


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date March 3, 2016
Est. primary completion date March 3, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

- healthy volunteer

Exclusion Criteria:

- smoker

- drug addiction

- significant neurological or psychiatric conditions

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
18F-PSS232
Diagnostic PET Tracer

Locations

Country Name City State
Switzerland University Hopsital Zurich Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference of Binding Potentials of 18F-PSS232 in different brain regions between Baseline PET and PET after medical challenge for details, please see Innis: Journal of Cerebral Blood Flow & Metabolism (2007) 27, 1533-1539 Baseline PET and PET after medical challenge will be scanned within 3 months
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