Informationen:
Fehler:
ID
39337
Beschreibung
A Prospective, Multicenter, Randomized, Open-label Study of 12 Week Duration to Evaluate the Effect of VILDagliptin Added to Insulin on Glycaemic Control in haemoDIALyzed Patients With Type 2 Diabetes: Probe Analysis of CGM; ODM derived from: https://clinicaltrials.gov/show/NCT02176681
Link
https://clinicaltrials.gov/show/NCT02176681
Stichworte
Versionen (1)
- 22.12.19 22.12.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
22. Dezember 2019
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Haemodialyzed, Type 2 Diabetes NCT02176681
Eligibility Haemodialyzed, Type 2 Diabetes NCT02176681
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Haemodialyzed, Type 2 Diabetes NCT02176681
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Hemodialysis | Glucose measurement Dialysis Solution
Item
patients treated by haemodialysis for more than 3 months with 1g/l glucose in dialysate fluid
boolean
C0019004 (UMLS CUI [1])
C0337438 (UMLS CUI [2,1])
C0011947 (UMLS CUI [2,2])
C0337438 (UMLS CUI [2,1])
C0011947 (UMLS CUI [2,2])
Insulin Dose Stable | Insulin regime Any Non-Insulin-Dependent Diabetes Mellitus | Antidiabetics Oral Absent
Item
patients treated by stable doses of insulin (any regimen) for type 2 diabetes without any oral antidiabetic agent
boolean
C0021641 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0557978 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
C0011860 (UMLS CUI [2,3])
C0935929 (UMLS CUI [3,1])
C1527415 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0557978 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
C0011860 (UMLS CUI [2,3])
C0935929 (UMLS CUI [3,1])
C1527415 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Age
Item
age > 18 and < 83 years
boolean
C0001779 (UMLS CUI [1])
Hemoglobin A1c measurement
Item
hba1c > 7%
boolean
C0474680 (UMLS CUI [1])
Erythropoietin Dose Variability | Blood Transfusion
Item
variability in epo doses > 20% of doses (u/kg/month) or blood transfusion in the 2 previous months
boolean
C0014822 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C2827666 (UMLS CUI [1,3])
C0005841 (UMLS CUI [2])
C0178602 (UMLS CUI [1,2])
C2827666 (UMLS CUI [1,3])
C0005841 (UMLS CUI [2])
Heart failure New York Heart Association Classification
Item
patients suffering from stage 3 and 4 cardiac insufficiency
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,2])
Life Expectancy
Item
life expectancy less than 1 year
boolean
C0023671 (UMLS CUI [1])
Chronic inflammatory disorder
Item
chronic inflammatory disease
boolean
C1290886 (UMLS CUI [1])
Steroid therapy
Item
steroid treatment
boolean
C0149783 (UMLS CUI [1])
Malignant Neoplasm Developmental | Malignant Neoplasm Requirement Chemotherapy | Malignant Neoplasm Requirement Therapeutic radiology procedure
Item
cancer (evolutive or requiring chemotherapy or radiotherapy)
boolean
C0006826 (UMLS CUI [1,1])
C0458003 (UMLS CUI [1,2])
C0006826 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0392920 (UMLS CUI [2,3])
C0006826 (UMLS CUI [3,1])
C1514873 (UMLS CUI [3,2])
C1522449 (UMLS CUI [3,3])
C0458003 (UMLS CUI [1,2])
C0006826 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0392920 (UMLS CUI [2,3])
C0006826 (UMLS CUI [3,1])
C1514873 (UMLS CUI [3,2])
C1522449 (UMLS CUI [3,3])
Patient scheduled for surgery
Item
patient waiting for programmed surgery
boolean
C3242215 (UMLS CUI [1])
Cardiovascular Disease | Cerebrovascular accident | Coronary heart disease | Hospitalization Due to Heart Failure
Item
history of cardiovascular disease (stroke, coronary heart disease, hospitalization for heart failure) in the 4 previous months
boolean
C0007222 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0010068 (UMLS CUI [3])
C3898876 (UMLS CUI [4])
C0038454 (UMLS CUI [2])
C0010068 (UMLS CUI [3])
C3898876 (UMLS CUI [4])
Patient Non-Compliance
Item
non-compliant patients
boolean
C0376405 (UMLS CUI [1])