Eligibility Diabetes Mellitus NCT01495052

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
all adults aged 50-65 years old with type 2 diabetes mellitus
Descripción

Adult | Age | Diabetes Mellitus, Non-Insulin-Dependent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
UMLS CUI [3]
C0011860
stable physical condition
Descripción

Physical Condition Stable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3714565
UMLS CUI [1,2]
C0205360
fasting plasma glucose (fpg) concentration ≥7.8mmol/l or 2-h postprandial blood glucose (pg) ≥11.1mmol/l after 75g oral dextrose with an glycated hemoglobin (hba1c)>7 %, stable medication.
Descripción

Plasma fasting glucose measurement | 2-hour postprandial blood glucose measurement | Status post Dextrose Oral Solution Dose Stable | Hemoglobin A1c measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0583513
UMLS CUI [2]
C2238058
UMLS CUI [3,1]
C0231290
UMLS CUI [3,2]
C2729678
UMLS CUI [3,3]
C0178602
UMLS CUI [3,4]
C0205360
UMLS CUI [4]
C0474680
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
breastfeeding
Descripción

Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006147
severe renal or hepatic complications
Descripción

Complication renal severe | Hepatic complications severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0022646
UMLS CUI [1,3]
C0205082
UMLS CUI [2,1]
C1832055
UMLS CUI [2,2]
C0205082
treatment by glucocorticoid
Descripción

Glucocorticoid therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0744425
having pancreatic disease or malignancy in recent 3 months
Descripción

Pancreatic Diseases | Malignant Neoplasms

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0030286
UMLS CUI [2]
C0006826
other factors that may limit adherence to interventions or affect conduct of the trial or participation in another supplementary feeding programme.
Descripción

Factor Limiting Adherence Intervention | Factor Affecting Completion of clinical trial | Participation Supplementary Feeding Program

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1521761
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C1510802
UMLS CUI [1,4]
C0184661
UMLS CUI [2,1]
C1521761
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C2732579
UMLS CUI [3,1]
C0679823
UMLS CUI [3,2]
C0038847
UMLS CUI [3,3]
C3484370

Similar models

Eligibility Diabetes Mellitus NCT01495052

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age | Diabetes Mellitus, Non-Insulin-Dependent
Item
all adults aged 50-65 years old with type 2 diabetes mellitus
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0011860 (UMLS CUI [3])
Physical Condition Stable
Item
stable physical condition
boolean
C3714565 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
Plasma fasting glucose measurement | 2-hour postprandial blood glucose measurement | Status post Dextrose Oral Solution Dose Stable | Hemoglobin A1c measurement
Item
fasting plasma glucose (fpg) concentration ≥7.8mmol/l or 2-h postprandial blood glucose (pg) ≥11.1mmol/l after 75g oral dextrose with an glycated hemoglobin (hba1c)>7 %, stable medication.
boolean
C0583513 (UMLS CUI [1])
C2238058 (UMLS CUI [2])
C0231290 (UMLS CUI [3,1])
C2729678 (UMLS CUI [3,2])
C0178602 (UMLS CUI [3,3])
C0205360 (UMLS CUI [3,4])
C0474680 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Breast Feeding
Item
breastfeeding
boolean
C0006147 (UMLS CUI [1])
Complication renal severe | Hepatic complications severe
Item
severe renal or hepatic complications
boolean
C0009566 (UMLS CUI [1,1])
C0022646 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C1832055 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Glucocorticoid therapy
Item
treatment by glucocorticoid
boolean
C0744425 (UMLS CUI [1])
Pancreatic Diseases | Malignant Neoplasms
Item
having pancreatic disease or malignancy in recent 3 months
boolean
C0030286 (UMLS CUI [1])
C0006826 (UMLS CUI [2])
Factor Limiting Adherence Intervention | Factor Affecting Completion of clinical trial | Participation Supplementary Feeding Program
Item
other factors that may limit adherence to interventions or affect conduct of the trial or participation in another supplementary feeding programme.
boolean
C1521761 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1510802 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,4])
C1521761 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C2732579 (UMLS CUI [2,3])
C0679823 (UMLS CUI [3,1])
C0038847 (UMLS CUI [3,2])
C3484370 (UMLS CUI [3,3])