ID

43931

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00087516

Trefwoorden

Versies (2)
  1. 30-08-16 30-08-16 -
  2. 20-09-21 20-09-21 -
Geüploaded op

20 september 2021

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Diabetes Mellitus, Type 2 NCT00087516

Engels

Eligibility Diabetes Mellitus, Type 2 NCT00087516

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with type 2 diabetes mellitus
Beschrijving

Diabetes Mellitus, Non-Insulin-Dependent

Datatype

boolean

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

Pregnancy | Breast Feeding

Datatype

boolean

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

Gender Fertility Unlikely

Datatype

boolean

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

Hypoglycemic Agents

Datatype

boolean

Alias
UMLS CUI [1]
C0020616
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Diabetes Mellitus, Insulin-Dependent

Datatype

boolean

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

Diabetic Ketoacidosis

Datatype

boolean

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

Insulin Patient need for

Datatype

boolean

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

Weight Reduction Program | Maintenance Phase

Datatype

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
Beschrijving

Weight-Loss Agents

Datatype

boolean

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

Adrenal Cortex Hormones | Adrenal Cortex Hormones Course Repeated

Datatype

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
Beschrijving

Immunosuppressive Agents | immunomodulating agent

Datatype

boolean

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

Digoxin | Cardiac agent

Datatype

boolean

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

General Anesthesia Related Operative Surgical Procedure

Datatype

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
Beschrijving

Investigational New Drugs

Datatype

boolean

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

Liver disease

Datatype

boolean

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

Myopathy chronic | nervous system disorder Progressive | Neuromuscular Disease Progressive

Datatype

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
Beschrijving

Heart Diseases Severe

Datatype

boolean

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

HIV Seropositivity

Datatype

boolean

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

Hematological Disease

Datatype

boolean

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

Malignant Neoplasms

Datatype

boolean

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

Substance Use Disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0038586
Terug naar het begin van de pagina

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00087516

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

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