ID
245
Beskrivning
ODM derived from http://clinicaltrials.gov/show/NCT00354627
Länk
http://clinicaltrials.gov/show/NCT00354627
Nyckelord
Versioner (3)
- 2012-03-13 2012-03-13 -
- 2014-04-14 2014-04-14 - Julian Varghese
- 2021-04-09 2021-04-09 - Ahmed Rafee, MD
Uppladdad den
13 mars 2012
DOI
För en begäran logga in.
Licens
Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT00354627 HIV-1
Eligibility
- StudyEvent: Eligibility
Beskrivning
Exclusion Criteria
Beskrivning
Prior or current participation in DUET trials (TMC125-C206 or TMC125-C216).
Datatyp
boolean
Alias
- UMLS CUI 2011AA
- C1516879
Beskrivning
Use of disallowed concomitant therapy, including disallowed antiretrovirals (ARV)
Datatyp
boolean
Alias
- UMLS CUI 2011AA
- C1444657
- SNOMED CT 2011_0131
- 410536001
- UMLS CUI 2011AA
- C0521115
- SNOMED CT 2011_0131
- 79970003
- UMLS CUI 2011AA
- C0039798
Beskrivning
Use of investigational ARVs (with exceptions)
Datatyp
boolean
Alias
- UMLS CUI 2011AA
- C0013230
Beskrivning
Any active clinically significant disease (e.g., cardiac dysfunction, pancreatitis, acute viral infection) or findings during screening of medical history or physical examination that is not either resolved or stabilized for at least 30 days before the Screening Phase
Datatyp
boolean
Alias
- UMLS CUI 2011AA
- C0205164
- SNOMED CT 2011_0131
- 255603008
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
Beskrivning
Pregnant or breast-feeding female
Datatyp
boolean
Alias
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C0006147
- MedDRA 14.1
- 10006247
Beskrivning
Female patient of childbearing potential not using effective non-hormonal birth control methods
Datatyp
boolean
Alias
- UMLS CUI 2011AA
- C0700589
- SNOMED CT 2011_0131
- 146680009
- MedDRA 14.1
- 10010808
Beskrivning
Patients with specific laboratory abnormalities
Datatyp
boolean
Beskrivning
Patients with clinical or laboratory evidence of significantly decreased hepatic function or decompensation.
Datatyp
boolean
Alias
- UMLS CUI 2011AA
- C1869009
- MedDRA 14.1
- 20000005
Similar models
Eligibility
- StudyEvent: Eligibility
397669002 (SNOMED CT 2011_0131)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0019693 (UMLS CUI 2011AA)
86406008 (SNOMED CT 2011_0131)
10020161 (MedDRA 14.1)
MTHU020829 (LOINC Version 232)
B20 (ICD-10-CM Version 2010)
042 (ICD-9-CM Version 2011)
C0013227 (UMLS CUI 2011AA)
C1527415 (UMLS CUI 2011AA)
26643006 (SNOMED CT 2011_0131)
_OralRoute (HL7 V3 2006_05)
C1963724 (UMLS CUI 2011AA)
10067326 (MedDRA 14.1)
MTHU000163 (LOINC Version 232)
C1373111 (UMLS CUI 2011AA)
C0033607 (UMLS CUI 2011AA)
412127001 (SNOMED CT 2011_0131)
C1373120 (UMLS CUI 2011AA)
C1373120 (UMLS CUI 2011AA)
C1373111 (UMLS CUI 2011AA)
C0033607 (UMLS CUI 2011AA)
412127001 (SNOMED CT 2011_0131)
412127001 (SNOMED CT 2011_0131)
10067326 (MedDRA 14.1)
MTHU000163 (LOINC Version 232)
C1320680 (UMLS CUI 2011AA)
405786003 (SNOMED CT 2011_0131)
410536001 (SNOMED CT 2011_0131)
C0521115 (UMLS CUI 2011AA)
79970003 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
255603008 (SNOMED CT 2011_0131)
C0012634 (UMLS CUI 2011AA)
64572001 (SNOMED CT 2011_0131)
10036586 (MedDRA 14.1)
C0006147 (UMLS CUI 2011AA)
10006247 (MedDRA 14.1)
146680009 (SNOMED CT 2011_0131)
10010808 (MedDRA 14.1)
20000005 (MedDRA 14.1)