ID

34603

Descripción

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

Link

https://clinicaltrials.gov/show/NCT01766752

Palabras clave

  1. 19/1/19 19/1/19 -
  2. 17/4/20 17/4/20 -
  3. 17/4/20 17/4/20 - Sarah Riepenhausen
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

19 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Type 2 Diabetes NCT01766752

Eligibility Type 2 Diabetes NCT01766752

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

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

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.4

Tipo de datos

boolean

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

ID.5

Tipo de datos

boolean

pregnancy
Descripción

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

terminally ill patients
Descripción

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

known or suspected allergy to insulin
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Type 2 Diabetes NCT01766752

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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