Eligibility Diabetes NCT01274364

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01274364
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetic patients attending hospitals or affiliated clinics led by pis of the jade program who are living in the area with an intention to have 'regular' follow-up
Description

Diabetes Mellitus, Non-Insulin-Dependent | Patients Attending Clinical Trial Hospital | Residence Clinical Trial Area | Follow-up Regular intended

Data type

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C1999232
UMLS CUI [2,3]
C0008976
UMLS CUI [2,4]
C0019994
UMLS CUI [3,1]
C0237096
UMLS CUI [3,2]
C0008976
UMLS CUI [3,3]
C0017446
UMLS CUI [4,1]
C3274571
UMLS CUI [4,2]
C0205272
UMLS CUI [4,3]
C1283828
aged >18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients can have newly diagnosed or established disease, treated with lifestyle or blood glucose lowering drugs including oral agents with or without insulin
Description

Disease Newly Diagnosed | Disease Established | Lifestyle Therapy | Hypoglycemic Agents | Oral medication | Insulin | Insulin Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1518321
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0443211
UMLS CUI [3]
C1517876
UMLS CUI [4]
C0020616
UMLS CUI [5]
C0175795
UMLS CUI [6]
C0021641
UMLS CUI [7,1]
C0021641
UMLS CUI [7,2]
C0332197
for newly diagnosed type 2 diabetic patients, their plasma glucose levels should be: a) fasting plasma glucose (pg) >7.0 mmol/l on 2 or more occasions, and/or b) random (or post-ogtt 2h) pg >11.1 mmol/l on 2 or more occasions, and/or c) hba1c >6.5%
Description

Non-Insulin-Dependent Diabetes Mellitus Newly Diagnosed | Plasma glucose level | Plasma fasting glucose measurement Number of occurrences | Plasma random glucose measurement Number of occurrences | Plasma Glucose Measurement Post Oral Glucose Tolerance Test | Hemoglobin A1c measurement

Data type

boolean

Alias
UMLS CUI [1,1]
C0011860
UMLS CUI [1,2]
C1518321
UMLS CUI [2]
C0455280
UMLS CUI [3,1]
C0583513
UMLS CUI [3,2]
C0449789
UMLS CUI [4,1]
C0583512
UMLS CUI [4,2]
C0449789
UMLS CUI [5,1]
C0202042
UMLS CUI [5,2]
C0687676
UMLS CUI [5,3]
C0029161
UMLS CUI [6]
C0474680
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
type 1 diabetes defined as a history of ketosis at diagnosis [acute symptoms with heavy ketonuria (>3+) or ketoacidosis] or continuous requirement of insulin within one year of diagnosis
Description

Diabetes Mellitus, Insulin-Dependent | Ketosis | Symptoms Ketonuria Severe | Symptoms Ketoacidosis | Requirement Insulin

Data type

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0022638
UMLS CUI [3,1]
C1457887
UMLS CUI [3,2]
C0162275
UMLS CUI [3,3]
C0205082
UMLS CUI [4,1]
C1457887
UMLS CUI [4,2]
C0220982
UMLS CUI [5,1]
C1514873
UMLS CUI [5,2]
C0021641
patients with reduced life expectancy (e.g. less than 6-months) due to recent diagnosis of advanced cancers (e.g. within last 2 years) and other life threatening conditions
Description

Reduced life expectancy Due to Advanced cancer | Condition Life Threatening

Data type

boolean

Alias
UMLS CUI [1,1]
C1858274
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0877373
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C2826244
patients with a mental condition rendering them unable to understand the nature, scope, and possible consequences of the study
Description

Study Protocol Comprehension Unable | Etiology Mental condition

Data type

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C0015127
UMLS CUI [2,2]
C3840291
patients actively enrolled in another intervention study
Description

Study Subject Participation Status | Interventional Study

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C3274035
patients who are unwilling to return for regular follow up
Description

Follow-up Regular Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0205272
UMLS CUI [1,3]
C0558080

Similar models

Eligibility Diabetes NCT01274364

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT01274364
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent | Patients Attending Clinical Trial Hospital | Residence Clinical Trial Area | Follow-up Regular intended
Item
type 2 diabetic patients attending hospitals or affiliated clinics led by pis of the jade program who are living in the area with an intention to have 'regular' follow-up
boolean
C0011860 (UMLS CUI [1])
C0030705 (UMLS CUI [2,1])
C1999232 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
C0019994 (UMLS CUI [2,4])
C0237096 (UMLS CUI [3,1])
C0008976 (UMLS CUI [3,2])
C0017446 (UMLS CUI [3,3])
C3274571 (UMLS CUI [4,1])
C0205272 (UMLS CUI [4,2])
C1283828 (UMLS CUI [4,3])
Age
Item
aged >18 years
boolean
C0001779 (UMLS CUI [1])
Disease Newly Diagnosed | Disease Established | Lifestyle Therapy | Hypoglycemic Agents | Oral medication | Insulin | Insulin Absent
Item
patients can have newly diagnosed or established disease, treated with lifestyle or blood glucose lowering drugs including oral agents with or without insulin
boolean
C0012634 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0012634 (UMLS CUI [2,1])
C0443211 (UMLS CUI [2,2])
C1517876 (UMLS CUI [3])
C0020616 (UMLS CUI [4])
C0175795 (UMLS CUI [5])
C0021641 (UMLS CUI [6])
C0021641 (UMLS CUI [7,1])
C0332197 (UMLS CUI [7,2])
Non-Insulin-Dependent Diabetes Mellitus Newly Diagnosed | Plasma glucose level | Plasma fasting glucose measurement Number of occurrences | Plasma random glucose measurement Number of occurrences | Plasma Glucose Measurement Post Oral Glucose Tolerance Test | Hemoglobin A1c measurement
Item
for newly diagnosed type 2 diabetic patients, their plasma glucose levels should be: a) fasting plasma glucose (pg) >7.0 mmol/l on 2 or more occasions, and/or b) random (or post-ogtt 2h) pg >11.1 mmol/l on 2 or more occasions, and/or c) hba1c >6.5%
boolean
C0011860 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0455280 (UMLS CUI [2])
C0583513 (UMLS CUI [3,1])
C0449789 (UMLS CUI [3,2])
C0583512 (UMLS CUI [4,1])
C0449789 (UMLS CUI [4,2])
C0202042 (UMLS CUI [5,1])
C0687676 (UMLS CUI [5,2])
C0029161 (UMLS CUI [5,3])
C0474680 (UMLS CUI [6])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent | Ketosis | Symptoms Ketonuria Severe | Symptoms Ketoacidosis | Requirement Insulin
Item
type 1 diabetes defined as a history of ketosis at diagnosis [acute symptoms with heavy ketonuria (>3+) or ketoacidosis] or continuous requirement of insulin within one year of diagnosis
boolean
C0011854 (UMLS CUI [1])
C0022638 (UMLS CUI [2])
C1457887 (UMLS CUI [3,1])
C0162275 (UMLS CUI [3,2])
C0205082 (UMLS CUI [3,3])
C1457887 (UMLS CUI [4,1])
C0220982 (UMLS CUI [4,2])
C1514873 (UMLS CUI [5,1])
C0021641 (UMLS CUI [5,2])
Reduced life expectancy Due to Advanced cancer | Condition Life Threatening
Item
patients with reduced life expectancy (e.g. less than 6-months) due to recent diagnosis of advanced cancers (e.g. within last 2 years) and other life threatening conditions
boolean
C1858274 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0877373 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C2826244 (UMLS CUI [2,2])
Study Protocol Comprehension Unable | Etiology Mental condition
Item
patients with a mental condition rendering them unable to understand the nature, scope, and possible consequences of the study
boolean
C2348563 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0015127 (UMLS CUI [2,1])
C3840291 (UMLS CUI [2,2])
Study Subject Participation Status | Interventional Study
Item
patients actively enrolled in another intervention study
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2])
Follow-up Regular Unwilling
Item
patients who are unwilling to return for regular follow up
boolean
C3274571 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])