Informações:
Falhas:
ID
15193
Descrição
DPP-4 Inhibitor and Serum BNP Level of Diabetic Patients With Congestive Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT02312427
Link
https://clinicaltrials.gov/show/NCT02312427
Palavras-chave
Versões (1)
- 22/05/2016 22/05/2016 -
Transferido a
22 de maio de 2016
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Heart Failure NCT02312427
Eligibility Heart Failure NCT02312427
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure NCT02312427
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
C0205250 (UMLS CUI [1,2])
Informed Consent
Item
patients who have given informed consent to participation in the study.
boolean
C0021430 (UMLS CUI [1])
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])
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])
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])
C1522541 (UMLS CUI [1,2])
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])
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])
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])
C0022423 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])