English

Eligibility Heart Failure NCT02312427

1 forms  
Criteria
Description

Criteria

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes patient with congestive heart failure under treatment with dpp-4 inhibitor (sitagliptin, vildagliptin, alogliptin, linagliptin, teneligliptin, anagliptin or saxagliptin) .
Description

Diabetes Mellitus, Non-Insulin-Dependent | Congestive heart failure | Therapeutic procedure Dipeptidyl Peptidase-4 Inhibitor | sitagliptin | vildagliptin | alogliptin | Linagliptin | teneligliptin | anagliptin | saxagliptin

Data type

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2]
C0018802
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C3537225
UMLS CUI [4]
C1565750
UMLS CUI [5]
C1570906
UMLS CUI [6]
C1958126
UMLS CUI [7]
C2746078
UMLS CUI [8]
C2981308
UMLS CUI [9]
C3272640
UMLS CUI [10]
C1611934
high serum bnp (100-2000pg/ml).
Description

B-type natriuretic peptide (BNP) High

Data type

boolean

Alias
UMLS CUI [1,1]
C2082356
UMLS CUI [1,2]
C0205250
patients who have given informed consent to participation in the study.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
hba1c over 9.0%.
Description

Glycosylated hemoglobin A

Data type

boolean

Alias
UMLS CUI [1]
C0019018
patients who changed medication within 1 months before inclusion.
Description

Change of medication Before Inclusion

Data type

boolean

Alias
UMLS CUI [1,1]
C0580105
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C1512693
judged as ineligible by clinical investigators.
Description

Ineligibility Judgment Clinical Investigators

Data type

boolean

Alias
UMLS CUI [1,1]
C1512714
UMLS CUI [1,2]
C0022423
UMLS CUI [1,3]
C0008961
hospitalization arm
Description

Hospitalization Arm

Data type

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C1522541
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes patient who were hospitalized for congestive heart failure.
Description

Diabetes Mellitus, Non-Insulin-Dependent | Hospitalization Congestive heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2,1]
C0019993
UMLS CUI [2,2]
C0018802
patients who have given informed consent to participation in the study.
Description

Informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients on insulin therapy.
Description

Insulin regime

Data type

boolean

Alias
UMLS CUI [1]
C0557978
judged as ineligible by clinical investigators.
Description

Ineligibility Judgment Clinical Investigators

Data type

boolean

Alias
UMLS CUI [1,1]
C1512714
UMLS CUI [1,2]
C0022423
UMLS CUI [1,3]
C0008961
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Similar models

Eligibility Heart Failure NCT02312427

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent | Congestive heart failure | Therapeutic procedure Dipeptidyl Peptidase-4 Inhibitor | sitagliptin | vildagliptin | alogliptin | Linagliptin | teneligliptin | anagliptin | saxagliptin
Item
type 2 diabetes patient with congestive heart failure under treatment with dpp-4 inhibitor (sitagliptin, vildagliptin, alogliptin, linagliptin, teneligliptin, anagliptin or saxagliptin) .
boolean
C0011860 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
C0087111 (UMLS CUI [3,1])
C3537225 (UMLS CUI [3,2])
C1565750 (UMLS CUI [4])
C1570906 (UMLS CUI [5])
C1958126 (UMLS CUI [6])
C2746078 (UMLS CUI [7])
C2981308 (UMLS CUI [8])
C3272640 (UMLS CUI [9])
C1611934 (UMLS CUI [10])
B-type natriuretic peptide (BNP) High
Item
high serum bnp (100-2000pg/ml).
boolean
C2082356 (UMLS CUI [1,1])
C0205250 (UMLS CUI [1,2])
Informed Consent
Item
patients who have given informed consent to participation in the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Glycosylated hemoglobin A
Item
hba1c over 9.0%.
boolean
C0019018 (UMLS CUI [1])
Change of medication Before Inclusion
Item
patients who changed medication within 1 months before inclusion.
boolean
C0580105 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C1512693 (UMLS CUI [1,3])
Ineligibility Judgment Clinical Investigators
Item
judged as ineligible by clinical investigators.
boolean
C1512714 (UMLS CUI [1,1])
C0022423 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
Hospitalization Arm
Item
hospitalization arm
boolean
C0019993 (UMLS CUI [1,1])
C1522541 (UMLS CUI [1,2])
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent | Hospitalization Congestive heart failure
Item
type 2 diabetes patient who were hospitalized for congestive heart failure.
boolean
C0011860 (UMLS CUI [1])
C0019993 (UMLS CUI [2,1])
C0018802 (UMLS CUI [2,2])
Informed consent
Item
patients who have given informed consent to participation in the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Insulin regime
Item
patients on insulin therapy.
boolean
C0557978 (UMLS CUI [1])
Ineligibility Judgment Clinical Investigators
Item
judged as ineligible by clinical investigators.
boolean
C1512714 (UMLS CUI [1,1])
C0022423 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
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