Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ChiCTR |
Last refreshed on:
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18 April 2017 |
Main ID: |
ChiCTR-OCB-15006947 |
Date of registration:
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2015-08-15 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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PET molecular imaging in the correlation study between the topological perception network and the default network
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Scientific title:
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PET molecular imaging in the correlation study between the topological perception network and the default network |
Date of first enrolment:
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2015-08-16 |
Target sample size:
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Healthy volunteer:60; |
Recruitment status: |
Pending |
URL:
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http://www.chictr.org.cn/showproj.aspx?proj=11653 |
Study type:
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Observational study |
Study design:
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historical control
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Phase:
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Diagnostic New Technique Clincal Study
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Countries of recruitment
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China
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Contacts
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Name:
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Haifeng Hou
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Address:
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88 Jiefang Road, Hangzhou, Zhejiang, China
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Telephone:
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+86 13767123896 |
Email:
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houhf@pku.edu.cn |
Affiliation:
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Second Affiliated Hospital of Zhejiang University School of Medicine |
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Name:
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Haifeng Hou
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Address:
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88 Jiefang Road, Hangzhou, Zhejiang, China
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Telephone:
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+86 13757123896 |
Email:
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houhf@pku.edu.cn |
Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1. Healthy volunteers with age between 18 to 25 years;
2. No history of physical, especially brain organic disease, and no history of substance use including analgesics, antiepileptics and antipsychotic;
3. No other serious concomitant diseases;
4. Willing and able to follow the program during the study period;
5. Written informed consent.
Exclusion criteria: 1. History of allergies to Contrast agents or tracers;
2. Having received any experimental drugs or protocols in half a year before entering the group , that is, having participated in another experiment;
3. current or past use of addictive drugs, analgesics, antiepileptics and antipsychotic;
4. Current or planned pregnancy;
5. Subjects receivied major surgery within 1 year before entering the group, or not yet fully recovered from the effects of major surgery;
6. Claustrophobic patients
7. Unwilling and unable to follow the program during the study period;
8. Current or past mood disorder, anxiety disorder, psychotic disorder, or mental retardation based on DSM-IV criteria.
Age minimum:
18
Age maximum:
25
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Topological perception network and the default network
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Intervention(s)
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Healthy volunteer:Topological picture;
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Primary Outcome(s)
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Cerebral perfusion;Cerebral glucose metabolism;
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Source(s) of Monetary Support
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Supporting funds for key disciplines of Zhejiang Province
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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