ID

5081

Descripción

ODM derived from http://clinicaltrials.gov/show/NCT01094678

Link

http://clinicaltrials.gov/show/NCT01094678

Palabras clave

  1. 6/12/13 6/12/13 - Martin Dugas
  2. 17/4/14 17/4/14 - Julian Varghese
Subido en

17 de abril de 2014

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility NCT01094678 Peripheral Arterial Disease

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Descripción

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Alter mindestens 18 Jahre
Descripción

age at least 18 Years

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0001779
SNOMED CT 2011_0131
397669002
stenosis of the above-the-knee femoropopliteal artery
Descripción

stenosis of the above-the-knee femoropopliteal artery

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C2721556
MedDRA 14.1
10069344
UMLS CUI 2011AA
C0011900
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
UMLS CUI 2011AA
CL384738
UMLS CUI 2011AA
C0022742
SNOMED CT 2011_0131
304679005
LOINC Version 232
MTHU002687
appropriate size and location of the lesion
Descripción

appropriate size and location of the lesion

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0814634
UMLS CUI 2011AA
C0449453
SNOMED CT 2011_0131
246116008
UMLS CUI 2011AA
C0450429
SNOMED CT 2011_0131
246267002
UMLS CUI 2011AA
C0221198
SNOMED CT 2011_0131
49755003
Ausschlusskriterien
Descripción

Ausschlusskriterien

Alias
UMLS CUI 2011AA
CL425201
pregnant or breast feeding
Descripción

pregnant or breast feeding

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0549206
MedDRA 14.1
10036586
UMLS CUI 2011AA
C0006147
MedDRA 14.1
10006247
failure or inability to give informed consent
Descripción

failure or inability to give informed consent

Tipo de datos

boolean

Alias
UMLS CUI 2011AA
C0021430
simultaneously participating in another drug or device study
Descripción

simultaneously participating in another drug or device study

Tipo de datos

boolean

Alias
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
C0013175
SNOMED CT 2011_0131
185922005
UMLS CUI 2011AA
C2346570
UMLS CUI 2011AA
C0008976
SNOMED CT 2011_0131
110465008

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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)
stenosis of the above-the-knee femoropopliteal artery
Item
stenosis of the above-the-knee femoropopliteal artery
boolean
C2721556 (UMLS CUI 2011AA)
10069344 (MedDRA 14.1)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
CL384738 (UMLS CUI 2011AA)
C0022742 (UMLS CUI 2011AA)
304679005 (SNOMED CT 2011_0131)
MTHU002687 (LOINC Version 232)
appropriate size and location of the lesion
Item
appropriate size and location of the lesion
boolean
C0814634 (UMLS CUI 2011AA)
C0449453 (UMLS CUI 2011AA)
246116008 (SNOMED CT 2011_0131)
C0450429 (UMLS CUI 2011AA)
246267002 (SNOMED CT 2011_0131)
C0221198 (UMLS CUI 2011AA)
49755003 (SNOMED CT 2011_0131)
Item Group
Ausschlusskriterien
CL425201 (UMLS CUI 2011AA)
pregnant or breast feeding
Item
pregnant or breast feeding
boolean
C0549206 (UMLS CUI 2011AA)
10036586 (MedDRA 14.1)
C0006147 (UMLS CUI 2011AA)
10006247 (MedDRA 14.1)
failure or inability to give informed consent
Item
failure or inability to give informed consent
boolean
C0021430 (UMLS CUI 2011AA)
simultaneously participating in another drug or device study
Item
simultaneously participating in another drug or device study
boolean
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)
C0013175 (UMLS CUI 2011AA)
185922005 (SNOMED CT 2011_0131)
C2346570 (UMLS CUI 2011AA)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)

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