ID

5081

Description

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

Link

http://clinicaltrials.gov/show/NCT01094678

Keywords

Versions (2)
  1. 12/6/13 12/6/13 - Martin Dugas
  2. 4/17/14 4/17/14 - Julian Varghese
Uploaded on

April 17, 2014

DOI

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License

Creative Commons BY 4.0
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Eligibility NCT01094678 Peripheral Arterial Disease

German English

Eligibility

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI 2011AA
CL425202
age at least 18 Years
Description

age at least 18 Years

Data type

boolean

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

stenosis of the above-the-knee femoropopliteal artery

Data type

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
Description

appropriate size and location of the lesion

Data type

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
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI 2011AA
CL425201
pregnant or breast feeding
Description

pregnant or breast feeding

Data type

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
Description

failure or inability to give informed consent

Data type

boolean

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

simultaneously participating in another drug or device study

Data type

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
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Similar models

Eligibility

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion Criteria
CL425202 (UMLS CUI 2011AA)
age at least 18 Years
Item
age at least 18 Years
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
Exclusion Criteria
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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