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Eligibility Chronic Kidney Disease NCT00396123

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
enrolled in university of michigan's nephrology anemia clinic
Description

Enrollment Nephrology clinic

Data type

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C3814531
18 years old or older
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
have kidney disease but are not on dialysis
Description

Kidney Disease Without Dialysis

Data type

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0332288
UMLS CUI [1,3]
C0011946
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
not enrolled in university of michigan's nephrology anemia clinic
Description

Enrollment Nephrology clinic

Data type

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C3814531
less than 18 years of age
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
hematocrit that is less than 28.5%
Description

Hematocrit procedure

Data type

boolean

Alias
UMLS CUI [1]
C0018935
currently participating in a clinical trial with an intervention
Description

Study Subject Participation Status | Clinical Trial Intervention

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C0184661
planning to change their tobacco use habits during the study period
Description

Tobacco use Habits Change Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C0543414
UMLS CUI [1,2]
C2242848
UMLS CUI [1,3]
C0392747
UMLS CUI [1,4]
C1301732
have had dose changes of certain medications for cholesterol or diabetes within one month of study enrollment
Description

Medication dose changed Cholesterol | Medication dose changed Diabetes Mellitus

Data type

boolean

Alias
UMLS CUI [1,1]
C1608430
UMLS CUI [1,2]
C0008377
UMLS CUI [2,1]
C1608430
UMLS CUI [2,2]
C0011849
are currently receiving:
Description

Patients Receive

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1514756
darbepoetin
Description

darbepoetin

Data type

boolean

Alias
UMLS CUI [1]
C0937950
erythopoietin
Description

Erythropoietin

Data type

boolean

Alias
UMLS CUI [1]
C0014822
medications to lower your immune system
Description

Pharmaceutical Preparations Immune system Lowering

Data type

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0020962
UMLS CUI [1,3]
C2003888
have had problems within the last 3 months with:
Description

Patient Problem

Data type

boolean

Alias
UMLS CUI [1]
C1254481
bleeding
Description

Hemorrhage

Data type

boolean

Alias
UMLS CUI [1]
C0019080
heart attack or stroke
Description

Myocardial Infarction | Cerebrovascular accident

Data type

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
heart or blood vessel procedures
Description

Procedure on heart | Procedure on blood vessel

Data type

boolean

Alias
UMLS CUI [1]
C1279986
UMLS CUI [2]
C1292969
are pregnant or lactating
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
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Similar models

Eligibility Chronic Kidney Disease NCT00396123

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Enrollment Nephrology clinic
Item
enrolled in university of michigan's nephrology anemia clinic
boolean
C1516879 (UMLS CUI [1,1])
C3814531 (UMLS CUI [1,2])
Age
Item
18 years old or older
boolean
C0001779 (UMLS CUI [1])
Kidney Disease Without Dialysis
Item
have kidney disease but are not on dialysis
boolean
C0022658 (UMLS CUI [1,1])
C0332288 (UMLS CUI [1,2])
C0011946 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Enrollment Nephrology clinic
Item
not enrolled in university of michigan's nephrology anemia clinic
boolean
C1516879 (UMLS CUI [1,1])
C3814531 (UMLS CUI [1,2])
Age
Item
less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
Hematocrit procedure
Item
hematocrit that is less than 28.5%
boolean
C0018935 (UMLS CUI [1])
Study Subject Participation Status | Clinical Trial Intervention
Item
currently participating in a clinical trial with an intervention
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
Tobacco use Habits Change Planned
Item
planning to change their tobacco use habits during the study period
boolean
C0543414 (UMLS CUI [1,1])
C2242848 (UMLS CUI [1,2])
C0392747 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,4])
Medication dose changed Cholesterol | Medication dose changed Diabetes Mellitus
Item
have had dose changes of certain medications for cholesterol or diabetes within one month of study enrollment
boolean
C1608430 (UMLS CUI [1,1])
C0008377 (UMLS CUI [1,2])
C1608430 (UMLS CUI [2,1])
C0011849 (UMLS CUI [2,2])
Patients Receive
Item
are currently receiving:
boolean
C0030705 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
darbepoetin
Item
darbepoetin
boolean
C0937950 (UMLS CUI [1])
Erythropoietin
Item
erythopoietin
boolean
C0014822 (UMLS CUI [1])
Pharmaceutical Preparations Immune system Lowering
Item
medications to lower your immune system
boolean
C0013227 (UMLS CUI [1,1])
C0020962 (UMLS CUI [1,2])
C2003888 (UMLS CUI [1,3])
Patient Problem
Item
have had problems within the last 3 months with:
boolean
C1254481 (UMLS CUI [1])
Hemorrhage
Item
bleeding
boolean
C0019080 (UMLS CUI [1])
Myocardial Infarction | Cerebrovascular accident
Item
heart attack or stroke
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Procedure on heart | Procedure on blood vessel
Item
heart or blood vessel procedures
boolean
C1279986 (UMLS CUI [1])
C1292969 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
are pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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