ID

43931

Beskrivning

Monotherapy Study in Patients With Type 2 Diabetes Mellitus (0431-021); ODM derived from: https://clinicaltrials.gov/show/NCT00087516

Länk

https://clinicaltrials.gov/show/NCT00087516

Nyckelord

  1. 2016-08-30 2016-08-30 -
  2. 2021-09-20 2021-09-20 -
Uppladdad den

20 september 2021

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT00087516

Eligibility Diabetes Mellitus, Type 2 NCT00087516

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with type 2 diabetes mellitus
Beskrivning

Diabetes Mellitus, Non-Insulin-Dependent

Datatyp

boolean

Alias
UMLS CUI [1]
C0011860
patient is not pregnant or breastfeeding
Beskrivning

Pregnancy | Breast Feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
male or female patient unlikely to conceive
Beskrivning

Gender Fertility Unlikely

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0015895
UMLS CUI [1,3]
C0750558
patient not on an antihyperglycemic drug
Beskrivning

Hypoglycemic Agents

Datatyp

boolean

Alias
UMLS CUI [1]
C0020616
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient has history of type 1 diabetes mellitus
Beskrivning

Diabetes Mellitus, Insulin-Dependent

Datatyp

boolean

Alias
UMLS CUI [1]
C0011854
patient has history of ketoacidosis
Beskrivning

Diabetic Ketoacidosis

Datatyp

boolean

Alias
UMLS CUI [1]
C0011880
patient requires insulin within 8 weeks prior to start of study
Beskrivning

Insulin Patient need for

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021641
UMLS CUI [1,2]
C0686904
patient on weight loss program and is not in maintenance phase
Beskrivning

Weight Reduction Program | Maintenance Phase

Datatyp

boolean

Alias
UMLS CUI [1]
C3179079
UMLS CUI [2,1]
C0024501
UMLS CUI [2,2]
C0205390
patient taking weight loss medication within 8 weeks prior to start of study
Beskrivning

Weight-Loss Agents

Datatyp

boolean

Alias
UMLS CUI [1]
C0376606
patient on or likely to require = 14 days or repeated courses of corticosteroids
Beskrivning

Adrenal Cortex Hormones | Adrenal Cortex Hormones Course Repeated

Datatyp

boolean

Alias
UMLS CUI [1]
C0001617
UMLS CUI [2,1]
C0001617
UMLS CUI [2,2]
C0750729
UMLS CUI [2,3]
C0205341
patient taking immunosuppressive/immunomodulating medication
Beskrivning

Immunosuppressive Agents | immunomodulating agent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021081
UMLS CUI [2]
C0005525
patient taking digoxin or other cardiac medication
Beskrivning

Digoxin | Cardiac agent

Datatyp

boolean

Alias
UMLS CUI [1]
C0012265
UMLS CUI [2]
C0007220
patient has undergone surgical general anesthesia within 30 days prior to start of study
Beskrivning

General Anesthesia Related Operative Surgical Procedure

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0002915
UMLS CUI [1,2]
C0439849
UMLS CUI [1,3]
C0543467
patient taking investigational drug within 8 weeks prior to start of study
Beskrivning

Investigational New Drugs

Datatyp

boolean

Alias
UMLS CUI [1]
C0013230
patient is diagnosed with liver disease
Beskrivning

Liver disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0023895
patient has chronic myopathy, progressive neurological/neuromuscular disorder
Beskrivning

Myopathy chronic | nervous system disorder Progressive | Neuromuscular Disease Progressive

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0026848
UMLS CUI [1,2]
C0205191
UMLS CUI [2,1]
C0027765
UMLS CUI [2,2]
C0205329
UMLS CUI [3,1]
C0027868
UMLS CUI [3,2]
C0205329
patient has with severe cardiac conditions within the last 6 months
Beskrivning

Heart Diseases Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205082
patient is human immunodeficiency virus (hiv) positive
Beskrivning

HIV Seropositivity

Datatyp

boolean

Alias
UMLS CUI [1]
C0019699
patient has hematological disorder
Beskrivning

Hematological Disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0018939
patient has history of malignancy
Beskrivning

Malignant Neoplasms

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
patient has history of alcohol or drug abuse within the past 3 years
Beskrivning

Substance Use Disorders

Datatyp

boolean

Alias
UMLS CUI [1]
C0038586

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00087516

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])

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