ID

16442

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT00328549

Nyckelord

  1. 2016-07-16 2016-07-16 -
Uppladdad den

16 juli 2016

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Hepatitis C NCT00328549

Eligibility Hepatitis C NCT00328549

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Beskrivning

signed informed consent

Datatyp

boolean

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

hcv- infected patients

Datatyp

boolean

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

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

Datatyp

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
Beskrivning

normal serum creatinine

Datatyp

boolean

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

life expectancy > 6 months

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
hiv-infected patients
Beskrivning

hiv-infected patients

Datatyp

boolean

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

history of any primary hematologic disease

Datatyp

boolean

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

attributable anemia

Datatyp

boolean

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

hemolysis or gastrointestinal bleeding

Datatyp

boolean

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

other hepatic disease

Datatyp

boolean

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

hcv

Datatyp

boolean

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

active substance use disorder

Datatyp

boolean

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

pregnant or breast feeding

Datatyp

boolean

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

birth control measures

Datatyp

boolean

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

epoetin alfa

Datatyp

boolean

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

recent transfusions

Datatyp

boolean

Alias
UMLS CUI [1]
C0005841

Similar models

Eligibility Hepatitis C NCT00328549

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

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