ID

22967

Description

Effect of Insulin Detemir on Use of Energy in Type 1 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00509925

Lien

https://clinicaltrials.gov/show/NCT00509925

Mots-clés

  1. 19/06/2017 19/06/2017 -
Téléchargé le

19 juin 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Diabetes NCT00509925

Eligibility Diabetes NCT00509925

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT00509925
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 1 diabetes for more than 12 months
Description

ID.1

Type de données

boolean

current treatment: basal-bolus insulin regimen for more than three months (i.e. at least one daily injection of long-acting insulin (including insulin glargine) and fast-acting insulin with each main meal)
Description

ID.2

Type de données

boolean

Alias
UMLS CUI [1]
C0557978
hba1c (glycosylated haemoglobin a1c) between 7.0 and 11.0%
Description

ID.3

Type de données

boolean

Alias
UMLS CUI [1]
C0019018
able and willing to maintain consistent physical activity level throughout the entire study period
Description

ID.4

Type de données

boolean

Alias
UMLS CUI [1]
C0015259
able and willing to maintain consistent eating habits throughout the entire study period
Description

ID.5

Type de données

boolean

Alias
UMLS CUI [1]
C1266864
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
proliferative retinopathy that has required acute treatment within the last six months
Description

ID.6

Type de données

boolean

Alias
UMLS CUI [1]
C0339467
recurrent major hypoglycaemia or hypoglycaemic unawareness as judged by the investigator
Description

ID.7

Type de données

boolean

Alias
UMLS CUI [1]
C0150254
liver, kidney or heart problems as judged by the investigator
Description

ID.8

Type de données

boolean

Alias
UMLS CUI [1]
C0012634
pregnancy, breast-feeding, the intention of becoming pregnant or not using adequate contraceptive measures
Description

ID.9

Type de données

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
UMLS CUI [1,3]
C0009862
known or suspected allergy to trial products or related products
Description

ID.10

Type de données

boolean

Alias
UMLS CUI [1]
C0020517
receipt of any investigational drug within one month prior to this trial
Description

ID.11

Type de données

boolean

Alias
UMLS CUI [1]
C0013230

Similar models

Eligibility Diabetes NCT00509925

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT00509925
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
type 1 diabetes for more than 12 months
boolean
ID.2
Item
current treatment: basal-bolus insulin regimen for more than three months (i.e. at least one daily injection of long-acting insulin (including insulin glargine) and fast-acting insulin with each main meal)
boolean
C0557978 (UMLS CUI [1])
ID.3
Item
hba1c (glycosylated haemoglobin a1c) between 7.0 and 11.0%
boolean
C0019018 (UMLS CUI [1])
ID.4
Item
able and willing to maintain consistent physical activity level throughout the entire study period
boolean
C0015259 (UMLS CUI [1])
ID.5
Item
able and willing to maintain consistent eating habits throughout the entire study period
boolean
C1266864 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.6
Item
proliferative retinopathy that has required acute treatment within the last six months
boolean
C0339467 (UMLS CUI [1])
ID.7
Item
recurrent major hypoglycaemia or hypoglycaemic unawareness as judged by the investigator
boolean
C0150254 (UMLS CUI [1])
ID.8
Item
liver, kidney or heart problems as judged by the investigator
boolean
C0012634 (UMLS CUI [1])
ID.9
Item
pregnancy, breast-feeding, the intention of becoming pregnant or not using adequate contraceptive measures
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0009862 (UMLS CUI [1,3])
ID.10
Item
known or suspected allergy to trial products or related products
boolean
C0020517 (UMLS CUI [1])
ID.11
Item
receipt of any investigational drug within one month prior to this trial
boolean
C0013230 (UMLS CUI [1])

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