Information:
Error:
ID
12775
Description
An Observational Study to Compare the Safety and Effectiveness of NovoMix® 30 and Levemir™ for the Treatment of Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00789711
Link
https://clinicaltrials.gov/show/NCT00789711
Keywords
Versions (1)
- 12/21/15 12/21/15 -
Uploaded on
December 21, 2015
DOI
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License
Creative Commons BY 4.0
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Eligibility Diabetes NCT00789711
Eligibility Diabetes NCT00789711
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes NCT00789711
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
diabetes mellitus
Item
patients diagnosed with type 1 or type 2 diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Antidiabetics Oral
Item
patients uncontrolled on oral antidiabetic drugs
boolean
C0935929 (UMLS CUI [1,1])
C0442027 (UMLS CUI [1,2])
C0442027 (UMLS CUI [1,2])
human insulin
Item
insulin naïve patients or patients currently on human insulin
boolean
C0020171 (UMLS CUI [1])
compliance
Item
subjects who are unlikely to comply with protocol requirements
boolean
C1321605 (UMLS CUI [1])
Study Subject Participation Status
Item
subjects who are previously enrolled in novomix® 30 and levemir™ study
boolean
C2348568 (UMLS CUI [1])
therapy novomix
Item
subjects on novomix® 30 and levemir™ therapy
boolean
C0087111 (UMLS CUI [1,1])
C1170447 (UMLS CUI [1,2])
C1170447 (UMLS CUI [1,2])
hypersensitivity novomix
Item
subjects with hypersensitivity to novomix® 30 or to any of the excipients
boolean
C0020517 (UMLS CUI [1,1])
C1170447 (UMLS CUI [1,2])
C1170447 (UMLS CUI [1,2])
hypersensitivity levemir
Item
subjects with hypersensitivity to levemir™ or to any of the excipients
boolean
C0020517 (UMLS CUI [1,1])
C1314782 (UMLS CUI [1,2])
C1314782 (UMLS CUI [1,2])
pregnant; contraceptive methods
Item
females of child bearing potential who are pregnant, breast feeding or intend to become pregnant or are not using adequate contraceptive methods (adequate contraceptive measures are required by local law or practice
boolean
C0549206 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0700589 (UMLS CUI [2])
contraindication
Item
contraindications and warnings specified in the current prescribing information
boolean
C1301624 (UMLS CUI [1])