Eligibility Chronic Kidney Disease NCT00396123

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Enrollment Nephrology clinic

Datatype

boolean

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

Age

Datatype

boolean

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

Kidney Disease Without Dialysis

Datatype

boolean

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

Exclusion Criteria

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

Enrollment Nephrology clinic

Datatype

boolean

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

Age

Datatype

boolean

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

Hematocrit procedure

Datatype

boolean

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

Study Subject Participation Status | Clinical Trial Intervention

Datatype

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
Beschrijving

Tobacco use Habits Change Planned

Datatype

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
Beschrijving

Medication dose changed Cholesterol | Medication dose changed Diabetes Mellitus

Datatype

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:
Beschrijving

Patients Receive

Datatype

boolean

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

darbepoetin

Datatype

boolean

Alias
UMLS CUI [1]
C0937950
erythopoietin
Beschrijving

Erythropoietin

Datatype

boolean

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

Pharmaceutical Preparations Immune system Lowering

Datatype

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:
Beschrijving

Patient Problem

Datatype

boolean

Alias
UMLS CUI [1]
C1254481
bleeding
Beschrijving

Hemorrhage

Datatype

boolean

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

Myocardial Infarction | Cerebrovascular accident

Datatype

boolean

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

Procedure on heart | Procedure on blood vessel

Datatype

boolean

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

Pregnancy | Breast Feeding

Datatype

boolean

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

Similar models

Eligibility Chronic Kidney Disease NCT00396123

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])