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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01045824
Other study ID # C08202
Secondary ID
Status Recruiting
Phase N/A
First received January 6, 2010
Last updated January 14, 2010
Start date January 2008
Est. completion date January 2014

Study information

Verified date January 2010
Source Taichung Veterans General Hospital
Contact Tsuo-Hung Lan, MD., PhD.
Phone 04-23592525
Email tosafish@hotmail.com
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

The goal of this research is to find out possible susceptible gene(s) in schizophrenic patients with family history and 5-year period functional changes of brain among the members of family, in order to further analysis factors and their interactions.


Description:

Schizophrenia is a serious mental disease, highly family inheritable inclination. By means of traditional psychiatry diagnosis, genetics and long term brain change researches will help to unveil the secret of schizophrenia and other factors. The advantage of comparative gene hybridization is that chromosome copy number alterations can be detected; this technique has been widely applied in many researches, such as cancer, mental retardation screening and autism. As we known, we are the first one use this technique in chromosome abnormality research for family history schizophrenic patient, this study also is the first one to track the relationship of long term brain function alteration and chromosome abnormality in Taiwan.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date January 2014
Est. primary completion date January 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

1.Psychiatry doctor diagnosed who met the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) criteria for schizophrenia or schizoaffective disorder, family history, age older than 15 will be recruited for participation in this study. Participants agree and sign informed consent forms will eligible to participate this experiment.

2.10-20c.c blood will be drawn from the participants. 3.Participants need to understand procedures and assays of this experiment. 4.At least one psychiatry doctor interview needed, participants and their family voluntarily join this interview, approximately 30-45min.

Exclusion Criteria:

1. Participant can not understand procedures and assays of this experiment.

2. Participant has another major mental disease other than the inclusion criteria.

3. Participant has material abuse history, it could seriously influence diagnosis.

4. Participant has combination diseases, it could seriously influence diagnosis.

5. Psychopathy or psychosis can not be categorized in defined group.

Other considerations:

1. Participants, age fewer than 20 needs to their deputy guardians (parents) and their own consent altogether.

2. Participants who are inability needs to their deputy guardians (parents) and their own consent altogether.

Study Design

Observational Model: Family-Based


Related Conditions & MeSH terms


Locations

Country Name City State
Taiwan Taichung Veterans General Hospital Taichung City

Sponsors (1)

Lead Sponsor Collaborator
Taichung Veterans General Hospital

Country where clinical trial is conducted

Taiwan, 

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