Informationen:
Fehler:
ID
20669
Beschreibung
LANTUSTITR: Insulin Glargine in Type 2 Diabetes Mellitus; ODM derived from: https://clinicaltrials.gov/show/NCT00349986
Link
https://clinicaltrials.gov/show/NCT00349986
Stichworte
Versionen (1)
- 09.03.17 09.03.17 -
Hochgeladen am
9. März 2017
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT00349986
Eligibility Diabetes Mellitus, Type 2 NCT00349986
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Diabetes Mellitus, Type 2 NCT00349986
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Diabetes Mellitus, Non-Insulin-Dependent
Item
type 2 diabetes mellitus
boolean
C0011860 (UMLS CUI [1])
Antidiabetics Oral Combined Insufficient | Biguanides | Sulfonylurea
Item
insufficient combined oral antidiabetic treatment (biguanide + sulfonylurea)
boolean
C0935929 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0205195 (UMLS CUI [1,3])
C0231180 (UMLS CUI [1,4])
C0005382 (UMLS CUI [2])
C0038766 (UMLS CUI [3])
C1527415 (UMLS CUI [1,2])
C0205195 (UMLS CUI [1,3])
C0231180 (UMLS CUI [1,4])
C0005382 (UMLS CUI [2])
C0038766 (UMLS CUI [3])
Body mass index
Item
bmi >25 kg/m2 , <30 kg/m2
boolean
C1305855 (UMLS CUI [1])
Glycosylated hemoglobin A Percentage
Item
hba1c value >7.0%, <9.0% within one month
boolean
C0019018 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,2])
Diabetes Mellitus, Insulin-Dependent
Item
type 1 diabetes mellitus
boolean
C0011854 (UMLS CUI [1])
Malignant Neoplasms
Item
known malignancy
boolean
C0006826 (UMLS CUI [1])
Substance Use Disorders
Item
drug or alcohol abuse
boolean
C0038586 (UMLS CUI [1])
Liver disease Severe
Item
severe liver disease
boolean
C0023895 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
Kidney Failure | Creatinine measurement, serum
Item
renal failure (se creatinine > 150 micro mol/l)
boolean
C0035078 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0201976 (UMLS CUI [2])
Study Subject Participation Status
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean
C2348568 (UMLS CUI [1])