Informationen:
Fehler:
ID
43931
Beschreibung
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
Stichworte
Versionen (2)
- 30.08.16 30.08.16 -
- 20.09.21 20.09.21 -
Hochgeladen am
20. September 2021
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Diabetes Mellitus, Type 2 NCT00087516
Eligibility Diabetes Mellitus, Type 2 NCT00087516
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Diabetes Mellitus, Type 2 NCT00087516
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
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])
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])
C0015895 (UMLS CUI [1,2])
C0750558 (UMLS CUI [1,3])
Hypoglycemic Agents
Item
patient not on an antihyperglycemic drug
boolean
C0020616 (UMLS CUI [1])
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])
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])
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])
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])
C0005525 (UMLS CUI [2])
Digoxin | Cardiac agent
Item
patient taking digoxin or other cardiac medication
boolean
C0012265 (UMLS CUI [1])
C0007220 (UMLS CUI [2])
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])
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])
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])
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])