ID

20543

Description

A Study of the Safety and Effectiveness of a R256918 in Patients With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00672386

Lien

https://clinicaltrials.gov/show/NCT00672386

Mots-clés

  1. 02/03/2017 02/03/2017 -
Téléchargé le

2 mars 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Diabetes Mellitus, Type 2 NCT00672386

Eligibility Diabetes Mellitus, Type 2 NCT00672386

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of type 2 diabetes mellitus and treated with a stable dose of metformin for at least 2 months
Description

type 2 diabetes mellitus, metformin

Type de données

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2]
C0025598
women must be postmenopausal or surgically incapable of childbearing or if sexually active, be practicing an effective method of birth control
Description

Gender | Postmenopausal state | Childbearing Potential | Contraceptive methods

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0232970
UMLS CUI [3]
C3831118
UMLS CUI [4]
C0700589
bmi between 25 and 45 kg/m2
Description

bmi

Type de données

boolean

Alias
UMLS CUI [1]
C1305855
hba1c between 7% and 10%, inclusive
Description

hba1c

Type de données

boolean

Alias
UMLS CUI [1]
C0019018
fasting plasma glucose not exceeding 240mg/dl (13.3mmol/l)
Description

fasting plasma glucose

Type de données

boolean

Alias
UMLS CUI [1]
C0583513
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
diabetes other than type 2 diabetes mellitus
Description

diabetes type

Type de données

boolean

Alias
UMLS CUI [1]
C1320657
treatment with oral anti-diabetic agents (other than metformin) or insulin during the 12 weeks before baseline visit
Description

oral hypoglycemic, insulin

Type de données

boolean

Alias
UMLS CUI [1]
C0359086
UMLS CUI [2]
C0021641
history of intolerance or hypersensitivity to sulfonylurea or sitagliptin
Description

intolerance or hypersensitivity to sulfonylurea or sitagliptin

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0038766
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C1565750
history of clinically significant gastrointestinal, hepatic or cardiovascular disease
Description

history of clinically significant gastrointestinal, hepatic or cardiovascular disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0009488
UMLS CUI [2]
C0017178
UMLS CUI [3]
C0023895
UMLS CUI [4]
C0007222
active proliferative diabetic retinopathy
Description

active proliferative diabetic retinopathy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0154830
UMLS CUI [1,2]
C0205177
history of diabetic gastroparesis
Description

diabetic gastroparesis

Type de données

boolean

Alias
UMLS CUI [1]
C0267176
concurrent use of systemic corticosteroid
Description

steroid therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0149783

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00672386

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
type 2 diabetes mellitus, metformin
Item
history of type 2 diabetes mellitus and treated with a stable dose of metformin for at least 2 months
boolean
C0011860 (UMLS CUI [1])
C0025598 (UMLS CUI [2])
Gender | Postmenopausal state | Childbearing Potential | Contraceptive methods
Item
women must be postmenopausal or surgically incapable of childbearing or if sexually active, be practicing an effective method of birth control
boolean
C0079399 (UMLS CUI [1])
C0232970 (UMLS CUI [2])
C3831118 (UMLS CUI [3])
C0700589 (UMLS CUI [4])
bmi
Item
bmi between 25 and 45 kg/m2
boolean
C1305855 (UMLS CUI [1])
hba1c
Item
hba1c between 7% and 10%, inclusive
boolean
C0019018 (UMLS CUI [1])
fasting plasma glucose
Item
fasting plasma glucose not exceeding 240mg/dl (13.3mmol/l)
boolean
C0583513 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
diabetes type
Item
diabetes other than type 2 diabetes mellitus
boolean
C1320657 (UMLS CUI [1])
oral hypoglycemic, insulin
Item
treatment with oral anti-diabetic agents (other than metformin) or insulin during the 12 weeks before baseline visit
boolean
C0359086 (UMLS CUI [1])
C0021641 (UMLS CUI [2])
intolerance or hypersensitivity to sulfonylurea or sitagliptin
Item
history of intolerance or hypersensitivity to sulfonylurea or sitagliptin
boolean
C0020517 (UMLS CUI [1,1])
C0038766 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1565750 (UMLS CUI [2,2])
history of clinically significant gastrointestinal, hepatic or cardiovascular disease
Item
history of clinically significant gastrointestinal, hepatic or cardiovascular disease
boolean
C0262926 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
C0017178 (UMLS CUI [2])
C0023895 (UMLS CUI [3])
C0007222 (UMLS CUI [4])
active proliferative diabetic retinopathy
Item
active proliferative diabetic retinopathy
boolean
C0154830 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
diabetic gastroparesis
Item
history of diabetic gastroparesis
boolean
C0267176 (UMLS CUI [1])
steroid therapy
Item
concurrent use of systemic corticosteroid
boolean
C0149783 (UMLS CUI [1])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial