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Information:
Fel:
ID
22748
Beskrivning
A Double-blind and Randomized Trial of Celecoxib Added to Risperidone in Treatment-naive First-episode Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00686140
Länk
https://clinicaltrials.gov/show/NCT00686140
Nyckelord
Versioner (2)
- 2017-06-11 2017-06-11 -
- 2021-09-20 2021-09-20 -
Uppladdad den
11 juni 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Schizophrenia NCT00686140
Eligibility Schizophrenia NCT00686140
- StudyEvent: Eligibility
Similar models
Eligibility Schizophrenia NCT00686140
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
schizophrenia, schizophreniform disorder
Item
diagnosis of schizophrenia or schizophreniform disorder;
boolean
C0036341 (UMLS CUI [1])
C0036358 (UMLS CUI [2])
C0036358 (UMLS CUI [2])
duration of symptoms
Item
duration of symptoms not longer than 60 months;
boolean
C0449238 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C1457887 (UMLS CUI [1,2])
prior therapy, antipsychotic medication
Item
no prior treatment with antipsychotic medication or, if previously treated, a total lifetime usage of less than 14 days;
boolean
C1514463 (UMLS CUI [1,1])
C0040615 (UMLS CUI [1,2])
C0040615 (UMLS CUI [1,2])
age
Item
between 16 and 40 years of age; and
boolean
C0001779 (UMLS CUI [1])
current psychotic symptoms of moderate severity
Item
current psychotic symptoms of moderate severity.
boolean
C0521116 (UMLS CUI [1,1])
C0871189 (UMLS CUI [1,2])
C0205081 (UMLS CUI [1,3])
C0871189 (UMLS CUI [1,2])
C0205081 (UMLS CUI [1,3])
dsm-iv axis i diagnosis other than schizophrenia or schizophreniform
Item
a dsm-iv axis i diagnosis other than schizophrenia or schizophreniform;
boolean
C0220952 (UMLS CUI [1,1])
C0270287 (UMLS CUI [1,2])
C0338607 (UMLS CUI [1,3])
C0270287 (UMLS CUI [1,2])
C0338607 (UMLS CUI [1,3])
central nervous system disease, stroke, tumor, parkinson's disease, huntington's disease, seizure disorder, history of brain trauma resulting in significant impairment, chronic infection
Item
documented disease of the central nervous system that can interfere with the trial assessments including, but not limited to stroke, tumor, parkinson's disease, huntington's disease, seizure disorder, history of brain trauma resulting in significant impairment, chronic, infection;
boolean
C0007682 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0085136 (UMLS CUI [3])
C0030567 (UMLS CUI [4])
C0020179 (UMLS CUI [5])
C0014544 (UMLS CUI [6])
C0876926 (UMLS CUI [7,1])
C0221099 (UMLS CUI [7,2])
C0151317 (UMLS CUI [8])
C0038454 (UMLS CUI [2])
C0085136 (UMLS CUI [3])
C0030567 (UMLS CUI [4])
C0020179 (UMLS CUI [5])
C0014544 (UMLS CUI [6])
C0876926 (UMLS CUI [7,1])
C0221099 (UMLS CUI [7,2])
C0151317 (UMLS CUI [8])
severe comorbidity
Item
acute, unstable and/or significant and untreated medical illness (e.g., infection, unstable diabetes, uncontrolled hypertension);
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
ecg abnormality
Item
a clinically significant ecg abnormality in the opinion of the investigator;
boolean
C1832603 (UMLS CUI [1])
pregnancy, breast feeding
Item
pregnant or breast-feeding female;
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0006147 (UMLS CUI [1,2])
disallowed concomitant therapy
Item
use of disallowed concomitant therapy;
boolean
C1707479 (UMLS CUI [1])
history of severe allergy or hypersensitivity
Item
history of severe allergy or hypersensitivity.
boolean
C0020517 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2945656 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C2945656 (UMLS CUI [2])