ID

39644

Description

Part A: Drug Interaction Study of Sofosbuvir and Antiretroviral Therapy (ART) Combinations in HIV and Hepatitis C Virus (HCV) Co-infected Patients. Part B: Efficacy and Safety of Sofosbuvir for 12 Weeks in HIV/HCV Co-infected Patients.; ODM derived from: https://clinicaltrials.gov/show/NCT01565889

Lien

https://clinicaltrials.gov/show/NCT01565889

Mots-clés

  1. 07/02/2020 07/02/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

7 février 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Hepatitis C NCT01565889

Eligibility Hepatitis C NCT01565889

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy according to medical history and physical examination with exception of hcv and hiv diagnoses
Description

Healthy Medical History | Healthy Physical Examination | Exception Hepatitis C | Exception HIV Infection

Type de données

boolean

Alias
UMLS CUI [1,1]
C3898900
UMLS CUI [1,2]
C0262926
UMLS CUI [2,1]
C3898900
UMLS CUI [2,2]
C0031809
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0019196
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0019693
confirmation of chronic hcv infection
Description

Hepatitis C, Chronic

Type de données

boolean

Alias
UMLS CUI [1]
C0524910
confirmation of chronic hiv-1 infection
Description

HIV-1 infection chronic

Type de données

boolean

Alias
UMLS CUI [1,1]
C2363741
UMLS CUI [1,2]
C0205191
on a stable protocol approved hiv antiretroviral (arv) regimen with undetectable hiv-rna
Description

HIV Antiretroviral therapy Stable | HIV RNA undetectable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019682
UMLS CUI [1,2]
C1963724
UMLS CUI [1,3]
C0205360
UMLS CUI [2]
C0877598
agree to use two forms of highly effective contraception for the duration of the study and 6 months after the last dose of study medication
Description

Contraceptive methods Quantity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C1265611
subjects must be naive to treatment for chronic hcv infection
Description

Therapy naive Chronic Hepatitis C

Type de données

boolean

Alias
UMLS CUI [1,1]
C0919936
UMLS CUI [1,2]
C0524910
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known or suspected cirrhosis
Description

Liver Cirrhosis | Liver Cirrhosis Suspected

Type de données

boolean

Alias
UMLS CUI [1]
C0023890
UMLS CUI [2,1]
C0023890
UMLS CUI [2,2]
C0750491
history of any other clinically significant chronic liver disease
Description

Chronic liver disease Other

Type de données

boolean

Alias
UMLS CUI [1,1]
C0341439
UMLS CUI [1,2]
C0205394
a history consistent with decompensated liver disease.
Description

Medical History Consistent with Decompensated liver disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0332290
UMLS CUI [1,3]
C4075847
use of any prohibited medications as defined by the protocol
Description

Illicit medication use

Type de données

boolean

Alias
UMLS CUI [1]
C0281875
pregnant or nursing female or male with pregnant female partner
Description

Pregnancy | Breast Feeding | Gender Partner Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C0079399
UMLS CUI [3,2]
C0682323
UMLS CUI [3,3]
C0032961
contraindication to peg or rbv therapy (for part b)
Description

Medical contraindication PEGINTERFERON Therapy | Medical contraindication Ribavirin Therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0982327
UMLS CUI [1,3]
C0087111
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0035525
UMLS CUI [2,3]
C0087111
clinically relevant drug or alcohol abuse
Description

Substance Use Disorders

Type de données

boolean

Alias
UMLS CUI [1]
C0038586

Similar models

Eligibility Hepatitis C NCT01565889

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Healthy Medical History | Healthy Physical Examination | Exception Hepatitis C | Exception HIV Infection
Item
healthy according to medical history and physical examination with exception of hcv and hiv diagnoses
boolean
C3898900 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C3898900 (UMLS CUI [2,1])
C0031809 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0019196 (UMLS CUI [3,2])
C1705847 (UMLS CUI [4,1])
C0019693 (UMLS CUI [4,2])
Hepatitis C, Chronic
Item
confirmation of chronic hcv infection
boolean
C0524910 (UMLS CUI [1])
HIV-1 infection chronic
Item
confirmation of chronic hiv-1 infection
boolean
C2363741 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
HIV Antiretroviral therapy Stable | HIV RNA undetectable
Item
on a stable protocol approved hiv antiretroviral (arv) regimen with undetectable hiv-rna
boolean
C0019682 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0877598 (UMLS CUI [2])
Contraceptive methods Quantity
Item
agree to use two forms of highly effective contraception for the duration of the study and 6 months after the last dose of study medication
boolean
C0700589 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Therapy naive Chronic Hepatitis C
Item
subjects must be naive to treatment for chronic hcv infection
boolean
C0919936 (UMLS CUI [1,1])
C0524910 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Liver Cirrhosis | Liver Cirrhosis Suspected
Item
known or suspected cirrhosis
boolean
C0023890 (UMLS CUI [1])
C0023890 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Chronic liver disease Other
Item
history of any other clinically significant chronic liver disease
boolean
C0341439 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Medical History Consistent with Decompensated liver disease
Item
a history consistent with decompensated liver disease.
boolean
C0262926 (UMLS CUI [1,1])
C0332290 (UMLS CUI [1,2])
C4075847 (UMLS CUI [1,3])
Illicit medication use
Item
use of any prohibited medications as defined by the protocol
boolean
C0281875 (UMLS CUI [1])
Pregnancy | Breast Feeding | Gender Partner Pregnancy
Item
pregnant or nursing female or male with pregnant female partner
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0682323 (UMLS CUI [3,2])
C0032961 (UMLS CUI [3,3])
Medical contraindication PEGINTERFERON Therapy | Medical contraindication Ribavirin Therapy
Item
contraindication to peg or rbv therapy (for part b)
boolean
C1301624 (UMLS CUI [1,1])
C0982327 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1301624 (UMLS CUI [2,1])
C0035525 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,3])
Substance Use Disorders
Item
clinically relevant drug or alcohol abuse
boolean
C0038586 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial