Informatie:
Fout:
ID
32009
Beschrijving
Efficacy and Safety of AVE1625 as a Co-treatment With Antipsychotic Therapy in Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00439634
Link
https://clinicaltrials.gov/show/NCT00439634
Trefwoorden
Versies (1)
- 11-10-18 11-10-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
11 oktober 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Schizophrenia NCT00439634
Eligibility Schizophrenia NCT00439634
- StudyEvent: Eligibility
Similar models
Eligibility Schizophrenia NCT00439634
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Outpatients | Schizophrenia | Age
Item
outpatients with diagnosis of schizophrenia (diagnosed ≤ 35 years of age).
boolean
C0029921 (UMLS CUI [1])
C0036341 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0036341 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
olanzapine | Risperidone | paliperidone | quetiapine | aripiprazole
Item
current treatment consisting exclusively of olanzapine, risperidone/paliperidone, quetiapine or aripiprazole monotherapy for at least 2 months.
boolean
C0171023 (UMLS CUI [1])
C0073393 (UMLS CUI [2])
C0753678 (UMLS CUI [3])
C0123091 (UMLS CUI [4])
C0299792 (UMLS CUI [5])
C0073393 (UMLS CUI [2])
C0753678 (UMLS CUI [3])
C0123091 (UMLS CUI [4])
C0299792 (UMLS CUI [5])
Hospitalization
Item
inpatient hospitalization within past 3 months.
boolean
C0019993 (UMLS CUI [1])
Residence short-term | Disease Instability
Item
residence at the current address < 3 months due to any instability in the disease.
boolean
C0237096 (UMLS CUI [1,1])
C0443303 (UMLS CUI [1,2])
C0012634 (UMLS CUI [2,1])
C1444783 (UMLS CUI [2,2])
C0443303 (UMLS CUI [1,2])
C0012634 (UMLS CUI [2,1])
C1444783 (UMLS CUI [2,2])
Depressive Symptoms
Item
presence of depressive symptoms.
boolean
C0086132 (UMLS CUI [1])
Violent behavior
Item
past history of clinically significant violent behavior.
boolean
C0424323 (UMLS CUI [1])
Substance Dependence | Substance Use Disorders
Item
substance dependence or abuse.
boolean
C0038580 (UMLS CUI [1])
C0038586 (UMLS CUI [2])
C0038586 (UMLS CUI [2])
Pregnancy | Breast Feeding | Gender Contraceptive methods Absent
Item
pregnant or breast-feeding women or women not protected by effective contraceptive method of birth control.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0700589 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Study Subject Participation Status Inappropriate
Item
the investigator will evaluate whether there are other reasons why a patient may not participate.
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,2])