ID

16442

Description

A Study to Evaluate the Erythropoietic Response in Hepatitis C Virus (HCV) Patients Receiving Combination Ribavirin (RBV)/Interferon (IFN) Therapy or RBV/PEG IFN (NATURAL HISTORY-HCV); ODM derived from: https://clinicaltrials.gov/show/NCT00328549

Lien

https://clinicaltrials.gov/show/NCT00328549

Mots-clés

  1. 16/07/2016 16/07/2016 -
Téléchargé le

16 juillet 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Hepatitis C NCT00328549

Eligibility Hepatitis C NCT00328549

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Description

signed informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
hcv- infected patients confirmed by pcr or branched dna (b-dna)
Description

hcv- infected patients

Type de données

boolean

Alias
UMLS CUI [1]
C3844790
scheduled to commence combination rbv/ifn or rbv/peg-ifn therapy on day 1
Description

scheduled to commence combination rbv/ifn or rbv/peg-ifn therapy on day 1

Type de données

boolean

Alias
UMLS CUI [1,1]
C0205539
UMLS CUI [1,2]
C1971490
UMLS CUI [2,1]
C0205539
UMLS CUI [2,2]
C0035525
UMLS CUI [2,3]
C0279030
normal serum creatinine
Description

normal serum creatinine

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
life expectancy > 6 months
Description

life expectancy > 6 months

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
hiv-infected patients
Description

hiv-infected patients

Type de données

boolean

Alias
UMLS CUI [1]
C0019699
history of any primary hematologic disease
Description

history of any primary hematologic disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018939
UMLS CUI [1,2]
C0277554
anemia attributable to factors such as iron or folate deficiency, pre-treatment
Description

attributable anemia

Type de données

boolean

Alias
UMLS CUI [1]
C0162316
UMLS CUI [2]
C0497165
hemolysis or gastrointestinal bleeding
Description

hemolysis or gastrointestinal bleeding

Type de données

boolean

Alias
UMLS CUI [1]
C0019054
UMLS CUI [2]
C0017181
has suspected or confirmed significant hepatic disease from an etiology other than
Description

other hepatic disease

Type de données

boolean

Alias
UMLS CUI [1]
C0023895
hcv (e.g. alcohol, hbv, autoimmune disease etc)
Description

hcv

Type de données

boolean

Alias
UMLS CUI [1]
C0220847
current, active substance abuser
Description

active substance use disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0038586
pregnant or breast feeding
Description

pregnant or breast feeding

Type de données

boolean

Alias
UMLS CUI [1,1]
C0549206
UMLS CUI [1,2]
C0006147
women of childbearing potential not taking adequate birth control measures
Description

birth control measures

Type de données

boolean

Alias
UMLS CUI [1]
C0700589
exposure to epoetin alfa within three (3) months prior to study enrollment or during study
Description

epoetin alfa

Type de données

boolean

Alias
UMLS CUI [1]
C0357126
transfusion within three (3) months prior to study entry
Description

recent transfusions

Type de données

boolean

Alias
UMLS CUI [1]
C0005841

Similar models

Eligibility Hepatitis C NCT00328549

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
signed informed consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
hcv- infected patients
Item
hcv- infected patients confirmed by pcr or branched dna (b-dna)
boolean
C3844790 (UMLS CUI [1])
scheduled to commence combination rbv/ifn or rbv/peg-ifn therapy on day 1
Item
scheduled to commence combination rbv/ifn or rbv/peg-ifn therapy on day 1
boolean
C0205539 (UMLS CUI [1,1])
C1971490 (UMLS CUI [1,2])
C0205539 (UMLS CUI [2,1])
C0035525 (UMLS CUI [2,2])
C0279030 (UMLS CUI [2,3])
normal serum creatinine
Item
normal serum creatinine
boolean
C0201976 (UMLS CUI [1])
life expectancy > 6 months
Item
life expectancy > 6 months
boolean
C0023671 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
hiv-infected patients
Item
hiv-infected patients
boolean
C0019699 (UMLS CUI [1])
history of any primary hematologic disease
Item
history of any primary hematologic disease
boolean
C0018939 (UMLS CUI [1,1])
C0277554 (UMLS CUI [1,2])
attributable anemia
Item
anemia attributable to factors such as iron or folate deficiency, pre-treatment
boolean
C0162316 (UMLS CUI [1])
C0497165 (UMLS CUI [2])
hemolysis or gastrointestinal bleeding
Item
hemolysis or gastrointestinal bleeding
boolean
C0019054 (UMLS CUI [1])
C0017181 (UMLS CUI [2])
other hepatic disease
Item
has suspected or confirmed significant hepatic disease from an etiology other than
boolean
C0023895 (UMLS CUI [1])
hcv
Item
hcv (e.g. alcohol, hbv, autoimmune disease etc)
boolean
C0220847 (UMLS CUI [1])
active substance use disorder
Item
current, active substance abuser
boolean
C0038586 (UMLS CUI [1])
pregnant or breast feeding
Item
pregnant or breast feeding
boolean
C0549206 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
birth control measures
Item
women of childbearing potential not taking adequate birth control measures
boolean
C0700589 (UMLS CUI [1])
epoetin alfa
Item
exposure to epoetin alfa within three (3) months prior to study enrollment or during study
boolean
C0357126 (UMLS CUI [1])
recent transfusions
Item
transfusion within three (3) months prior to study entry
boolean
C0005841 (UMLS CUI [1])

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