ID

34213

Description

Effects of Hyperglycemia on Myocardial Perfusion in Humans With and Without Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01021865

Lien

https://clinicaltrials.gov/show/NCT01021865

Mots-clés

  1. 15/01/2019 15/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

15 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Coronary Artery Disease NCT01021865

Eligibility Coronary Artery Disease NCT01021865

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females
Description

ID.1

Type de données

boolean

age 40-60 years
Description

ID.2

Type de données

boolean

bmi< or = 35 kg/m2
Description

ID.3

Type de données

boolean

diabetic subjects with hba1c concentrations of < or = 8%.
Description

ID.4

Type de données

boolean

diabetic subjects will be either on diet and lifestyle therapy alone, or monotherapy with metformin or sulphonylureas (except glyburide).
Description

ID.5

Type de données

boolean

all diabetic subjects should be on stable dose oral agent therapy for 3 months prior to enrollment.
Description

ID.6

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with cerebrovascular or peripheral vascular disease.
Description

ID.7

Type de données

boolean

subjects with suspected or overt autonomic neuropathy.
Description

ID.8

Type de données

boolean

diabetic subject on thiazolidinediones, insulin, glp-1 based therapies (exenatide or sitagliptin), alpha-glucosidase inhibitors, glyburide or combination antidiabetic drug therapies.
Description

ID.9

Type de données

boolean

diabetics with microalbuminuria.
Description

ID.10

Type de données

boolean

Similar models

Eligibility Coronary Artery Disease NCT01021865

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
males and females
boolean
ID.2
Item
age 40-60 years
boolean
ID.3
Item
bmi< or = 35 kg/m2
boolean
ID.4
Item
diabetic subjects with hba1c concentrations of < or = 8%.
boolean
ID.5
Item
diabetic subjects will be either on diet and lifestyle therapy alone, or monotherapy with metformin or sulphonylureas (except glyburide).
boolean
ID.6
Item
all diabetic subjects should be on stable dose oral agent therapy for 3 months prior to enrollment.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
subjects with cerebrovascular or peripheral vascular disease.
boolean
ID.8
Item
subjects with suspected or overt autonomic neuropathy.
boolean
ID.9
Item
diabetic subject on thiazolidinediones, insulin, glp-1 based therapies (exenatide or sitagliptin), alpha-glucosidase inhibitors, glyburide or combination antidiabetic drug therapies.
boolean
ID.10
Item
diabetics with microalbuminuria.
boolean

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