Eligibility Diabetes Mellitus, Type 2 NCT00087516

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent
Item
patients with type 2 diabetes mellitus
boolean
C0011860 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
patient is not pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Gender Fertility Unlikely
Item
male or female patient unlikely to conceive
boolean
C0079399 (UMLS CUI [1,1])
C0015895 (UMLS CUI [1,2])
C0750558 (UMLS CUI [1,3])
Hypoglycemic Agents
Item
patient not on an antihyperglycemic drug
boolean
C0020616 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent
Item
patient has history of type 1 diabetes mellitus
boolean
C0011854 (UMLS CUI [1])
Diabetic Ketoacidosis
Item
patient has history of ketoacidosis
boolean
C0011880 (UMLS CUI [1])
Insulin Patient need for
Item
patient requires insulin within 8 weeks prior to start of study
boolean
C0021641 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
Weight Reduction Program | Maintenance Phase
Item
patient on weight loss program and is not in maintenance phase
boolean
C3179079 (UMLS CUI [1])
C0024501 (UMLS CUI [2,1])
C0205390 (UMLS CUI [2,2])
Weight-Loss Agents
Item
patient taking weight loss medication within 8 weeks prior to start of study
boolean
C0376606 (UMLS CUI [1])
Adrenal Cortex Hormones | Adrenal Cortex Hormones Course Repeated
Item
patient on or likely to require = 14 days or repeated courses of corticosteroids
boolean
C0001617 (UMLS CUI [1])
C0001617 (UMLS CUI [2,1])
C0750729 (UMLS CUI [2,2])
C0205341 (UMLS CUI [2,3])
Immunosuppressive Agents | immunomodulating agent
Item
patient taking immunosuppressive/immunomodulating medication
boolean
C0021081 (UMLS CUI [1])
C0005525 (UMLS CUI [2])
Digoxin | Cardiac agent
Item
patient taking digoxin or other cardiac medication
boolean
C0012265 (UMLS CUI [1])
C0007220 (UMLS CUI [2])
General Anesthesia Related Operative Surgical Procedure
Item
patient has undergone surgical general anesthesia within 30 days prior to start of study
boolean
C0002915 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,3])
Investigational New Drugs
Item
patient taking investigational drug within 8 weeks prior to start of study
boolean
C0013230 (UMLS CUI [1])
Liver disease
Item
patient is diagnosed with liver disease
boolean
C0023895 (UMLS CUI [1])
Myopathy chronic | nervous system disorder Progressive | Neuromuscular Disease Progressive
Item
patient has chronic myopathy, progressive neurological/neuromuscular disorder
boolean
C0026848 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0027765 (UMLS CUI [2,1])
C0205329 (UMLS CUI [2,2])
C0027868 (UMLS CUI [3,1])
C0205329 (UMLS CUI [3,2])
Heart Diseases Severe
Item
patient has with severe cardiac conditions within the last 6 months
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
HIV Seropositivity
Item
patient is human immunodeficiency virus (hiv) positive
boolean
C0019699 (UMLS CUI [1])
Hematological Disease
Item
patient has hematological disorder
boolean
C0018939 (UMLS CUI [1])
Malignant Neoplasms
Item
patient has history of malignancy
boolean
C0006826 (UMLS CUI [1])
Substance Use Disorders
Item
patient has history of alcohol or drug abuse within the past 3 years
boolean
C0038586 (UMLS CUI [1])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial