Schizophrenia Clinical Trial
— SELECTOfficial title:
24-Week Naturalistic Observational Study of Efficacy of Quetiapine in Patients With Schizophrenia or Schizoaffective Disorder
Verified date | August 2007 |
Source | AstraZeneca |
Contact | n/a |
Is FDA regulated | No |
Health authority | Korea: Food and Drug Administration |
Study type | Observational |
To assess the efficacy of 24-week treatment with quetiapine in patients with schizophrenia or schizoaffective disorder
Status | Completed |
Enrollment | 1000 |
Est. completion date | May 2008 |
Est. primary completion date | November 2007 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - The patient and the patient's legal representative (if any) must understand the nature of the study and must have given written consent - The patient suffers from schizophrenia or schizoaffective disorder according to DSM-IV-TR - The patient is between 18 and 65 years old(extremes included) - On the basis of physical and neurological examination, medical history, the patient is, in the investigator's opinion, otherwise healthy - If the subject is a female of childbearing potential, she must be not pregnant or breast-feeding and be using a reliable method of contraception. Reliable methods may include abstinence, hormonal contraceptives (eg,oral contraceptives or long-term injectable or implantable hormonal contraceptives), double-barrier methods (eg, condom and diaphragm, condom and foam, condom and sponge), intrauterine devices, and tubal ligation Exclusion Criteria: - The patients who have known hypersensitivity to quetiapine |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Research Site | Seoul | Dongdamoon-gu |
Korea, Republic of | Research Site | Seoul | Kangnam-gu |
Korea, Republic of | Research Site | Seoul | Songpa-gu |
Lead Sponsor | Collaborator |
---|---|
AstraZeneca |
Korea, Republic of,
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