ID
42777
Description
Safety and Efficacy Study of LB80380 in the Patients With Lamivudine-Refractory Chronic Hepatitis B; ODM derived from: https://clinicaltrials.gov/show/NCT00895596
Lien
https://clinicaltrials.gov/show/NCT00895596
Mots-clés
Versions (2)
- 03/08/2016 03/08/2016 -
- 17/09/2021 17/09/2021 -
Téléchargé le
17 septembre 2021
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Chronic Hepatitis B NCT00895596
Eligibility Chronic Hepatitis B NCT00895596
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
co-infection with hepatitis c or d virus (hcv or hdv) or hiv
Type de données
boolean
Alias
- UMLS CUI [1]
- C0275524
- UMLS CUI [2]
- C0220847
- UMLS CUI [3]
- C0011220
- UMLS CUI [4]
- C0019682
Description
pregnancy or breastfeeding
Type de données
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
treatment with nucleoside analogue or any other treatment for hbv
Type de données
boolean
Alias
- UMLS CUI [1]
- C1579410
- UMLS CUI [2,1]
- C0019163
- UMLS CUI [2,2]
- C0013227
Description
immunomodulatory agent or corticosteroids
Type de données
boolean
Alias
- UMLS CUI [1]
- C0005525
- UMLS CUI [2]
- C0001617
Description
decompensated liver disease
Type de données
boolean
Alias
- UMLS CUI [1]
- C4075847
Description
screening alpha-fetoprotein (afp), ultrasonography, indicative of hcc
Type de données
boolean
Alias
- UMLS CUI [1]
- C0201539
- UMLS CUI [2]
- C0041618
- UMLS CUI [3]
- C2239176
Description
anti-hbs
Type de données
boolean
Alias
- UMLS CUI [1]
- C0201478
Similar models
Eligibility Chronic Hepatitis B NCT00895596
- StudyEvent: Eligibility
C0205432 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2,1])
C0205432 (UMLS CUI [2,2])
C0220847 (UMLS CUI [2])
C0011220 (UMLS CUI [3])
C0019682 (UMLS CUI [4])
C0006147 (UMLS CUI [2])
C0019163 (UMLS CUI [2,1])
C0013227 (UMLS CUI [2,2])
C0001617 (UMLS CUI [2])
C0041618 (UMLS CUI [2])
C2239176 (UMLS CUI [3])
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