ID

34603

Description

Performance of a Tablet Based Workflow and Decision Support System With Incorporated Software Algorithm Used for Glycaemic Management; ODM derived from: https://clinicaltrials.gov/show/NCT01766752

Lien

https://clinicaltrials.gov/show/NCT01766752

Mots-clés

  1. 19/01/2019 19/01/2019 -
  2. 17/04/2020 17/04/2020 -
  3. 17/04/2020 17/04/2020 - Sarah Riepenhausen
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

19 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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Eligibility Type 2 Diabetes NCT01766752

Eligibility Type 2 Diabetes NCT01766752

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
informed consent obtained after being advised of the nature of the study
Description

ID.1

Type de données

boolean

male or female aged 18 - 90 years (both inclusive)
Description

ID.2

Type de données

boolean

type 2 diabetes treated with diet, oral agents, non-insulin injected anti-diabetic medicine, insulin therapy or any combination of the four
Description

ID.3

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
impaired renal function (serum creatinine ≥3.0mg/dl)
Description

ID.4

Type de données

boolean

any disease or condition which the investigator or treating physician feels would interfere with the trial or the safety of the patient
Description

ID.5

Type de données

boolean

pregnancy
Description

ID.6

Type de données

boolean

any mental condition rendering the patient incapable of giving his consent
Description

ID.7

Type de données

boolean

terminally ill patients
Description

ID.8

Type de données

boolean

participation in a trial within 3 months prior to this trial
Description

ID.9

Type de données

boolean

known or suspected allergy to insulin
Description

ID.10

Type de données

boolean

Similar models

Eligibility Type 2 Diabetes NCT01766752

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
informed consent obtained after being advised of the nature of the study
boolean
ID.2
Item
male or female aged 18 - 90 years (both inclusive)
boolean
ID.3
Item
type 2 diabetes treated with diet, oral agents, non-insulin injected anti-diabetic medicine, insulin therapy or any combination of the four
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
impaired renal function (serum creatinine ≥3.0mg/dl)
boolean
ID.5
Item
any disease or condition which the investigator or treating physician feels would interfere with the trial or the safety of the patient
boolean
ID.6
Item
pregnancy
boolean
ID.7
Item
any mental condition rendering the patient incapable of giving his consent
boolean
ID.8
Item
terminally ill patients
boolean
ID.9
Item
participation in a trial within 3 months prior to this trial
boolean
ID.10
Item
known or suspected allergy to insulin
boolean

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