ID

4510

Beskrivning

ODM derived from http://clinicaltrials.gov/show/NCT00635492

Länk

http://clinicaltrials.gov/show/NCT00635492

Nyckelord

Versioner (1)
  1. 2013-12-09 2013-12-09 - Martin Dugas
Uppladdad den

9 december 2013

DOI

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Creative Commons BY 4.0
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Eligibility NCT00635492 Type 2 Diabetes Mellitus

Tysk Engelsk

Eligibility

1 Formulär  
  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Beskrivning

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Alter mindestens 18 Jahre
Beskrivning

age at least 18 Years

Datatyp

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
diagnosed with type 2 diabetes
Beskrivning

diagnosed with type 2 diabetes

Datatyp

boolean

Alias
UMLS CUI 2011AA
C0011860
SNOMED CT 2011_0131
44054006
MedDRA 14.1
10012613
ICD-10-CM Version 2010
E08-E13
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
have had a treatment decision made within the normal course of care to initiate either insulin or exenatide for the treatment of type 2 diabetes
Beskrivning

have had a treatment decision made within the normal course of care to initiate either insulin or exenatide for the treatment of type 2 diabetes

Datatyp

boolean

Alias
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C0679006
UMLS CUI 2011AA
C0750729
SNOMED CT 2011_0131
288524001
UMLS CUI 2011AA
C0496675
UMLS CUI 2011AA
C1704686
UMLS CUI 2011AA
C0021641
SNOMED CT 2011_0131
67866001
LOINC Version 232
MTHU019392
UMLS CUI 2011AA
C0167117
SNOMED CT 2011_0131
416859008
UMLS CUI 2011AA
C0039798
UMLS CUI 2011AA
C0011860
SNOMED CT 2011_0131
44054006
MedDRA 14.1
10012613
ICD-10-CM Version 2010
E08-E13
have not previously been treated with either insulin or exenatide
Beskrivning

have not previously been treated with either insulin or exenatide

Datatyp

boolean

Alias
UMLS CUI 2011AA
C1518422
UMLS CUI 2011AA
C1514463
UMLS CUI 2011AA
C0021641
SNOMED CT 2011_0131
67866001
LOINC Version 232
MTHU019392
UMLS CUI 2011AA
C0167117
SNOMED CT 2011_0131
416859008
are not simultaneously participating in another study which includes an investigational drug or procedure at study entry
Beskrivning

are not simultaneously participating in another study which includes an investigational drug or procedure at study entry

Datatyp

boolean

Alias
UMLS CUI 2011AA
C1518422
UMLS CUI 2011AA
C0521115
SNOMED CT 2011_0131
79970003
UMLS CUI 2011AA
C0679823
HL7 V3 2006_05
PART
UMLS CUI 2011AA
C0205394
SNOMED CT 2011_0131
74964007
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008
UMLS CUI 2011AA
C0332257
SNOMED CT 2011_0131
55919000
UMLS CUI 2011AA
C0013230
UMLS CUI 2011AA
C1517586
UMLS CUI 2011AA
C2700391
UMLS CUI 2011AA
C2348558
have been fully informed and given their written consent for use of their data
Beskrivning

have been fully informed and given their written consent for use of their data

Datatyp

boolean

Alias
UMLS CUI 2011AA
C1576874
HL7 V3 2006_05
WRITTEN
UMLS CUI 2011AA
C0021430
UMLS CUI 2011AA
C1524063
SNOMED CT 2011_0131
260676000
UMLS CUI 2011AA
C1511726
have sufficient understanding of the primary language of their country such that they will be able to complete the questionnaires.
Beskrivning

have sufficient understanding of the primary language of their country such that they will be able to complete the questionnaires.

Datatyp

boolean

Alias
UMLS CUI 2011AA
C0205410
SNOMED CT 2011_0131
51117008
UMLS CUI 2011AA
C0162340
SNOMED CT 2011_0131
66216009
UMLS CUI 2011AA
CL414904
UMLS CUI 2011AA
C0023008
SNOMED CT 2011_0131
61909002
LOINC Version 232
MTHU021113
UMLS CUI 2011AA
C0454664
SNOMED CT 2011_0131
223369002
UMLS CUI 2011AA
C0085732
SNOMED CT 2011_0131
371150009
UMLS CUI 2011AA
C1554962
HL7 V3 2006_05
C
UMLS CUI 2011AA
C0034394
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Similar models

Eligibility

1 Formulär
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Einschlusskriterien
CL425202 (UMLS CUI 2011AA)
age at least 18 Years
Item
Alter mindestens 18 Jahre
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
diagnosed with type 2 diabetes
Item
diagnosed with type 2 diabetes
boolean
C0011860 (UMLS CUI 2011AA)
44054006 (SNOMED CT 2011_0131)
10012613 (MedDRA 14.1)
E08-E13 (ICD-10-CM Version 2010)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
have had a treatment decision made within the normal course of care to initiate either insulin or exenatide for the treatment of type 2 diabetes
Item
have had a treatment decision made within the normal course of care to initiate either insulin or exenatide for the treatment of type 2 diabetes
boolean
C0039798 (UMLS CUI 2011AA)
C0679006 (UMLS CUI 2011AA)
C0750729 (UMLS CUI 2011AA)
288524001 (SNOMED CT 2011_0131)
C0496675 (UMLS CUI 2011AA)
C1704686 (UMLS CUI 2011AA)
C0021641 (UMLS CUI 2011AA)
67866001 (SNOMED CT 2011_0131)
MTHU019392 (LOINC Version 232)
C0167117 (UMLS CUI 2011AA)
416859008 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C0011860 (UMLS CUI 2011AA)
44054006 (SNOMED CT 2011_0131)
10012613 (MedDRA 14.1)
E08-E13 (ICD-10-CM Version 2010)
have not previously been treated with either insulin or exenatide
Item
have not previously been treated with either insulin or exenatide
boolean
C1518422 (UMLS CUI 2011AA)
C1514463 (UMLS CUI 2011AA)
C0021641 (UMLS CUI 2011AA)
67866001 (SNOMED CT 2011_0131)
MTHU019392 (LOINC Version 232)
C0167117 (UMLS CUI 2011AA)
416859008 (SNOMED CT 2011_0131)
are not simultaneously participating in another study which includes an investigational drug or procedure at study entry
Item
are not simultaneously participating in another study which includes an investigational drug or procedure at study entry
boolean
C1518422 (UMLS CUI 2011AA)
C0521115 (UMLS CUI 2011AA)
79970003 (SNOMED CT 2011_0131)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C0332257 (UMLS CUI 2011AA)
55919000 (SNOMED CT 2011_0131)
C0013230 (UMLS CUI 2011AA)
C1517586 (UMLS CUI 2011AA)
C2700391 (UMLS CUI 2011AA)
C2348558 (UMLS CUI 2011AA)
have been fully informed and given their written consent for use of their data
Item
have been fully informed and given their written consent for use of their data
boolean
C1576874 (UMLS CUI 2011AA)
WRITTEN (HL7 V3 2006_05)
C0021430 (UMLS CUI 2011AA)
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C1511726 (UMLS CUI 2011AA)
have sufficient understanding of the primary language of their country such that they will be able to complete the questionnaires.
Item
have sufficient understanding of the primary language of their country such that they will be able to complete the questionnaires.
boolean
C0205410 (UMLS CUI 2011AA)
51117008 (SNOMED CT 2011_0131)
C0162340 (UMLS CUI 2011AA)
66216009 (SNOMED CT 2011_0131)
CL414904 (UMLS CUI 2011AA)
C0023008 (UMLS CUI 2011AA)
61909002 (SNOMED CT 2011_0131)
MTHU021113 (LOINC Version 232)
C0454664 (UMLS CUI 2011AA)
223369002 (SNOMED CT 2011_0131)
C0085732 (UMLS CUI 2011AA)
371150009 (SNOMED CT 2011_0131)
C1554962 (UMLS CUI 2011AA)
C (HL7 V3 2006_05)
C0034394 (UMLS CUI 2011AA)
Tillbaka till toppen 

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