Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Diabetes Mellitus, Non-Insulin-Dependent | Antidiabetics Protocol Required
Item
diagnosed with type 2 diabetes and treated with diabetes medication(s) as required by the protocol (see section 3.1)
boolean
C0011860 (UMLS CUI [1])
C0935929 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C1514873 (UMLS CUI [2,3])
Age
Item
age 18 and older
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
willing to give informed consent
boolean
C0021430 (UMLS CUI [1])
Adherence Study Protocol | Adherence Instructions Research Personnel
Item
motivated and capable of following the protocol and instructions provided by the healthcare professional
boolean
C1510802 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C1510802 (UMLS CUI [2,1])
C1442085 (UMLS CUI [2,2])
C0035173 (UMLS CUI [2,3])
Patient Available Clinical Trial | Patient Available Clinic Visits
Item
available for the study on the scheduled visit days
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0470187 (UMLS CUI [2,2])
C0008952 (UMLS CUI [2,3])
Participation Absent Clinical Trial Continuous glucose monitoring
Item
have not participated in a prior research trial at idc that utilized cgm
boolean
C0679823 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C4523945 (UMLS CUI [1,4])
Age
Item
under 18 years of age
boolean
C0001779 (UMLS CUI [1])
Skin Abnormalities Continuous glucose monitoring Site
Item
skin abnormalities at the cgm insertion sites that would confound assessment of the effect of the device on the skin
boolean
C0037268 (UMLS CUI [1,1])
C4523945 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
Allergy to adhesive
Item
allergy to adhesives
boolean
C1635164 (UMLS CUI [1])
Prednisone | Cortisone
Item
taken prednisone or cortisone medications in the previous 30 days
boolean
C0032952 (UMLS CUI [1])
C0010137 (UMLS CUI [2])
Pregnancy | Pregnancy, Planned
Item
currently pregnant or planning pregnancy during the study period
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Medical condition Severe compromises Patient safety | Mental condition Severe compromises Patient safety | Chronic condition compromises Patient safety | Chronic infectious disease compromises Patient safety | Medical condition Severe compromises Study Subject Participation Status | Mental condition Severe compromises Study Subject Participation Status | Chronic condition compromises Study Subject Participation Status | Chronic infectious disease compromises Study Subject Participation Status
Item
presence of any severe medical or psychological condition or chronic conditions/infections that in the opinion of the investigator would compromise the subject's safety or successful participation in the study
boolean
C3843040 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2945640 (UMLS CUI [1,3])
C1113679 (UMLS CUI [1,4])
C3840291 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C2945640 (UMLS CUI [2,3])
C1113679 (UMLS CUI [2,4])
C4315615 (UMLS CUI [3,1])
C2945640 (UMLS CUI [3,2])
C1113679 (UMLS CUI [3,3])
C0151317 (UMLS CUI [4,1])
C2945640 (UMLS CUI [4,2])
C1113679 (UMLS CUI [4,3])
C3843040 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C2945640 (UMLS CUI [5,3])
C2348568 (UMLS CUI [5,4])
C3840291 (UMLS CUI [6,1])
C0205082 (UMLS CUI [6,2])
C2945640 (UMLS CUI [6,3])
C2348568 (UMLS CUI [6,4])
C4315615 (UMLS CUI [7,1])
C2945640 (UMLS CUI [7,2])
C2348568 (UMLS CUI [7,3])
C0151317 (UMLS CUI [8,1])
C2945640 (UMLS CUI [8,2])
C2348568 (UMLS CUI [8,3])
Protocol Compliance Unable
Item
unable to follow the study protocol
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Lacking Able to speak English Language | Lacking Able to read English Language | Lacking Able to write English Language
Item
unable to speak, read and write in english
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0586740 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
C0332268 (UMLS CUI [3,1])
C0584993 (UMLS CUI [3,2])
C0376245 (UMLS CUI [3,3])