Informações:
Falhas:
ID
25590
Descrição
Characteristics of Glargine in Type 2 Diabetics; ODM derived from: https://clinicaltrials.gov/show/NCT00574912
Link
https://clinicaltrials.gov/show/NCT00574912
Palavras-chave
Versões (1)
- 07/09/2017 07/09/2017 -
Transferido a
7 de setembro de 2017
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 Type 2 Diabetes NCT00574912
Eligibility Type 2 Diabetes NCT00574912
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes NCT00574912
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Adult Quantity | Non-Insulin-Dependent Diabetes Mellitus disease length | Oral medication | Sulfonylureas | Metformin | Acarbose | Glinides | Insulin
Item
12 adults (males or females) with type 2 diabetes for at least six (6) months. may be using oral agents (sus, metformin, acarbose or glitinides) with or without insulin.
boolean
C0001675 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0011860 (UMLS CUI [2,1])
C0872146 (UMLS CUI [2,2])
C0175795 (UMLS CUI [3])
C0038766 (UMLS CUI [4])
C0025598 (UMLS CUI [5])
C0050393 (UMLS CUI [6])
C3537178 (UMLS CUI [7])
C0021641 (UMLS CUI [8])
C1265611 (UMLS CUI [1,2])
C0011860 (UMLS CUI [2,1])
C0872146 (UMLS CUI [2,2])
C0175795 (UMLS CUI [3])
C0038766 (UMLS CUI [4])
C0025598 (UMLS CUI [5])
C0050393 (UMLS CUI [6])
C3537178 (UMLS CUI [7])
C0021641 (UMLS CUI [8])
Glycosylated hemoglobin A
Item
hgba1c 7 -12%
boolean
C0019018 (UMLS CUI [1])
Age
Item
age 18-70 years
boolean
C0001779 (UMLS CUI [1])
Body mass index
Item
bmi 27-40 kg/m²
boolean
C1305855 (UMLS CUI [1])
Abnormality Study Subject Participation Status Inappropriate | Medical condition Study Subject Participation Status Inappropriate | Circumstances Study Subject Participation Status Inappropriate
Item
any past or present clinically relevant abnormality, medical condition, or circumstance making the subject unsuitable for participation in the study
boolean
C1704258 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C1548788 (UMLS CUI [2,3])
C0680082 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C1548788 (UMLS CUI [3,3])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C1548788 (UMLS CUI [2,3])
C0680082 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C1548788 (UMLS CUI [3,3])
Liver Failure | Kidney Failure | Heart failure
Item
evidence of hepatic, renal or cardiac failure
boolean
C0085605 (UMLS CUI [1])
C0035078 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
C0035078 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
Screening tests Abnormal results
Item
abnormal results following screening tests
boolean
C0871311 (UMLS CUI [1,1])
C0459424 (UMLS CUI [1,2])
C0459424 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Childbearing Potential Sexual Abstinence Unwilling | Childbearing Potential Contraceptive methods
Item
pregnant or lactating females or females of childbearing potential who are unwilling to abstain from sexual intercourse or use reliable, medically accepted methods of contraception
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0036899 (UMLS CUI [3,2])
C0558080 (UMLS CUI [3,3])
C3831118 (UMLS CUI [4,1])
C0700589 (UMLS CUI [4,2])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0036899 (UMLS CUI [3,2])
C0558080 (UMLS CUI [3,3])
C3831118 (UMLS CUI [4,1])
C0700589 (UMLS CUI [4,2])
Thiazolidinediones
Item
currently using tzds
boolean
C1257987 (UMLS CUI [1])
Alcoholic Intoxication, Chronic | Drug abuse
Item
history of alcoholism or drug abuse within 12 months of the study
boolean
C0001973 (UMLS CUI [1])
C0013146 (UMLS CUI [2])
C0013146 (UMLS CUI [2])