ID

25590

Description

Characteristics of Glargine in Type 2 Diabetics; ODM derived from: https://clinicaltrials.gov/show/NCT00574912

Lien

https://clinicaltrials.gov/show/NCT00574912

Mots-clés

Versions (1)
  1. 07/09/2017 07/09/2017 -
Téléchargé le

7 septembre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Type 2 Diabetes NCT00574912

Anglais

Eligibility Type 2 Diabetes NCT00574912

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
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.
Description

Adult Quantity | Non-Insulin-Dependent Diabetes Mellitus disease length | Oral medication | Sulfonylureas | Metformin | Acarbose | Glinides | Insulin

Type de données

boolean

Alias
UMLS CUI [1,1]
C0001675
UMLS CUI [1,2]
C1265611
UMLS CUI [2,1]
C0011860
UMLS CUI [2,2]
C0872146
UMLS CUI [3]
C0175795
UMLS CUI [4]
C0038766
UMLS CUI [5]
C0025598
UMLS CUI [6]
C0050393
UMLS CUI [7]
C3537178
UMLS CUI [8]
C0021641
hgba1c 7 -12%
Description

Glycosylated hemoglobin A

Type de données

boolean

Alias
UMLS CUI [1]
C0019018
age 18-70 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
bmi 27-40 kg/m²
Description

Body mass index

Type de données

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any past or present clinically relevant abnormality, medical condition, or circumstance making the subject unsuitable for participation in the study
Description

Abnormality Study Subject Participation Status Inappropriate | Medical condition Study Subject Participation Status Inappropriate | Circumstances Study Subject Participation Status Inappropriate

Type de données

boolean

Alias
UMLS CUI [1,1]
C1704258
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C1548788
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C1548788
UMLS CUI [3,1]
C0680082
UMLS CUI [3,2]
C2348568
UMLS CUI [3,3]
C1548788
evidence of hepatic, renal or cardiac failure
Description

Liver Failure | Kidney Failure | Heart failure

Type de données

boolean

Alias
UMLS CUI [1]
C0085605
UMLS CUI [2]
C0035078
UMLS CUI [3]
C0018801
abnormal results following screening tests
Description

Screening tests Abnormal results

Type de données

boolean

Alias
UMLS CUI [1,1]
C0871311
UMLS CUI [1,2]
C0459424
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
Description

Pregnancy | Breast Feeding | Childbearing Potential Sexual Abstinence Unwilling | Childbearing Potential Contraceptive methods

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C3831118
UMLS CUI [3,2]
C0036899
UMLS CUI [3,3]
C0558080
UMLS CUI [4,1]
C3831118
UMLS CUI [4,2]
C0700589
currently using tzds
Description

Thiazolidinediones

Type de données

boolean

Alias
UMLS CUI [1]
C1257987
history of alcoholism or drug abuse within 12 months of the study
Description

Alcoholic Intoxication, Chronic | Drug abuse

Type de données

boolean

Alias
UMLS CUI [1]
C0001973
UMLS CUI [2]
C0013146
Retour au début de la page

Similar models

Eligibility Type 2 Diabetes NCT00574912

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
Screening tests Abnormal results
Item
abnormal results following screening tests
boolean
C0871311 (UMLS CUI [1,1])
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])
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])
Retour au début de la page 

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