Information:
Fel:
ID
34287
Beskrivning
Comparing Efficacy and Safety of Insulin Detemir Plus Insulin Aspart and NPH Insulin Plus Human Soluble Insulin With or Without Metformin in Chinese Patients With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01486966
Länk
https://clinicaltrials.gov/show/NCT01486966
Nyckelord
Versioner (1)
- 2019-01-16 2019-01-16 -
Rättsinnehavare
see on clinicaltrials.gov
Uppladdad den
16 januari 2019
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Diabetes NCT01486966
Eligibility Diabetes NCT01486966
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes NCT01486966
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
ID.1
Item
type 2 diabetes mellitus (diagnosed clinically) for at 12 months or longer
boolean
ID.2
Item
currently treated with basal insulin once daily or premixed insulin twice daily for at least 3 months with or without oad(s), and total daily insulin dose less than 1.4 iu (u)/kg (if treated with metformin, unchanged total daily dose of at least 1000 mg for at least 3 months)
boolean
ID.3
Item
body mass index (bmi) equal to 40 kg/m^2 or below
boolean
ID.4
Item
hba1c (glycosylated haemoglobin a1c) between 7.0% and 10.0% by central laboratory analysis
boolean
ID.5
Item
plan to be admitted for optimising glycaemic control at least 2 days prior to the randomisation
boolean
ID.6
Item
treatment with thiazolidinediones (tzd) or glucagon-like peptide-1 (glp-1) receptor agonists within the last 3 months prior to the screening
boolean
ID.7
Item
anticipated change after the randomisation in concomitant medication known to interfere with glucose metabolism, such as systemic corticosteroids, beta-blockers and mono amine oxidase (mao) inhibitors
boolean
ID.8
Item
previous participation in this trial (participation is defined as randomised. re-screening of screening failures is allowed only once within the limits of the recruitment period.)
boolean