ID
245
Description
ODM derived from http://clinicaltrials.gov/show/NCT00354627
Lien
http://clinicaltrials.gov/show/NCT00354627
Mots-clés
Versions (3)
- 13/03/2012 13/03/2012 -
- 14/04/2014 14/04/2014 - Julian Varghese
- 09/04/2021 09/04/2021 - Ahmed Rafee, MD
Téléchargé le
13 mars 2012
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0 Legacy
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Eligibility NCT00354627 HIV-1
Eligibility
- StudyEvent: Eligibility
Description
Ausschlusskriterien
Description
Prior or current participation in DUET trials (TMC125-C206 or TMC125-C216).
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C1516879
Description
Use of disallowed concomitant therapy, including disallowed antiretrovirals (ARV)
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C1444657
- SNOMED CT 2011_0131
- 410536001
- UMLS CUI 2011AA
- C0521115
- SNOMED CT 2011_0131
- 79970003
- UMLS CUI 2011AA
- C0039798
Description
Use of investigational ARVs (with exceptions)
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0013230
Description
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
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0205164
- SNOMED CT 2011_0131
- 255603008
- UMLS CUI 2011AA
- C0012634
- SNOMED CT 2011_0131
- 64572001
Description
Pregnant or breast-feeding female
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C0006147
- MedDRA 14.1
- 10006247
Description
Female patient of childbearing potential not using effective non-hormonal birth control methods
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0700589
- SNOMED CT 2011_0131
- 146680009
- MedDRA 14.1
- 10010808
Description
Patients with specific laboratory abnormalities
Type de données
boolean
Description
Patients with clinical or laboratory evidence of significantly decreased hepatic function or decompensation.
Type de données
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)