Diabetes Mellitus, Non-Insulin-Dependent
Item
patients diagnosed as having type 2 diabetes.
boolean
C0011860 (UMLS CUI [1])
Insulin regime Absent
Item
patients who have not been on insulin treatment within 6 months.
boolean
C0557978 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Antidiabetics Oral
Item
patients who have been taking oads for at least 90 days.
boolean
C0935929 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
Glucohemoglobin measurement
Item
patients with an hba1c level in the range of 7.5% to 11.0%.
boolean
C0202054 (UMLS CUI [1])
Body mass index
Item
patients with a body-mass index (bmi) of 35 kg/m² or below.
boolean
C1305855 (UMLS CUI [1])
Preproliferative diabetic retinopathy | Proliferative retinopathy | Exception Retinal Disease No treatment required for
Item
patients having pre-proliferative or proliferative retinopathy (except for old retinopathy with no need for treatment).
boolean
C0339473 (UMLS CUI [1])
C0339467 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0035309 (UMLS CUI [3,2])
C0332126 (UMLS CUI [3,3])
Malignant Neoplasms | Malignant Neoplasms Suspected
Item
patients having or suspected of having malignancy
boolean
C0006826 (UMLS CUI [1])
C0006826 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Cardiac complication Serious | Hepatic complications Serious | Kidney complications Serious
Item
patients having serious complications of the heart, liver, or kidney.
boolean
C0161816 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C1832055 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C1408259 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
Insulin allergy | Hypersensitivity Insulin Analog
Item
patients hypersensitive or allergic to insulin or insulin analog preparations or a history of it.
boolean
C0571622 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C2825028 (UMLS CUI [2,2])
Systemic steroids
Item
patients receiving systemic steroids.
boolean
C2825233 (UMLS CUI [1])
Study Subject Participation Status | Drugs, Non-Prescription | Post marketing study
Item
are currently enrolled in a clinical trial of a non-approved drug. or patients who participated in other clinical trials including post-marketing clinical trials within 90 days prior to informed consent being obtained.
boolean
C2348568 (UMLS CUI [1])
C0013231 (UMLS CUI [2])
C1548594 (UMLS CUI [3])
Childbearing Potential | Breast Feeding | Childbearing Potential Pregnancy test positive
Item
patients of child-bearing potential. breastfeeding patients. patients with a positive result in a pregnancy test performed for women of child-bearing potential.
boolean
C3831118 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0240802 (UMLS CUI [3,2])