ID
5047
Description
ODM derived from http://clinicaltrials.gov/show/NCT00923754
Link
http://clinicaltrials.gov/show/NCT00923754
Keywords
Versions (2)
- 12/9/13 12/9/13 - Martin Dugas
- 4/17/14 4/17/14 - Julian Varghese
Uploaded on
April 17, 2014
DOI
To request one please log in.
License
Creative Commons BY 4.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Eligibility NCT00923754 Descending Thoracic Aortic Aneurysm
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Description
Age < 18 years
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0001779
- SNOMED CT 2011_0131
- 397669002
Description
Other medical condition that may cause the patient to be non-compliant with the protocol, confound the results, or is associated with limited life expectancy (i.e., < 2 years)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1699700
- HL7 V3 2006_05
- MEDCCAT
- UMLS CUI 2011AA
- C0457432
- SNOMED CT 2011_0131
- 258143003
- UMLS CUI 2011AA
- C2348563
- UMLS CUI 2011AA
- C0521102
- SNOMED CT 2011_0131
- 78235001
- UMLS CUI 2011AA
- C1274040
- SNOMED CT 2011_0131
- 79409006
- UMLS CUI 2011AA
- C0449295
- SNOMED CT 2011_0131
- 246175000
- UMLS CUI 2011AA
- C0023671
- LOINC Version 232
- LP75025-4
Description
Pregnant, breast-feeding, or planning on becoming pregnant within 24 months
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C0006147
- MedDRA 14.1
- 10006247
- UMLS CUI 2011AA
- C0032992
- SNOMED CT 2011_0131
- 169565003
Description
Unwilling or unable to comply with the follow-up schedule
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1522577
Description
Inability or refusal to give informed consent
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0021430
Description
< 30 days beyond primary endpoint in another investigative device or drug study
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C2346570
- UMLS CUI 2011AA
- C0013230
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
Similar models
Eligibility
- StudyEvent: Eligibility
397669002 (SNOMED CT 2011_0131)
10070725 (MedDRA 14.1)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
261399002 (SNOMED CT 2011_0131)
C0162872 (UMLS CUI 2011AA)
433068007 (SNOMED CT 2011_0131)
10043465 (MedDRA 14.1)
I71.2 (ICD-10-CM Version 2010)
441.2 (ICD-9-CM Version 2011)
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0220844 (UMLS CUI 2011AA)
32672002 (SNOMED CT 2011_0131)
MTHU007857 (LOINC Version 232)
C1880269 (UMLS CUI 2011AA)
C0004153 (UMLS CUI 2011AA)
38716007 (SNOMED CT 2011_0131)
10003601 (MedDRA 14.1)
I70 (ICD-10-CM Version 2010)
440 (ICD-9-CM Version 2011)
C0041582 (UMLS CUI 2011AA)
10045285 (SNOMED CT 2011_0131)
10045285 (MedDRA 14.1)
MTHU022920 (LOINC Version 232)
397669002 (SNOMED CT 2011_0131)
MEDCCAT (HL7 V3 2006_05)
C0457432 (UMLS CUI 2011AA)
258143003 (SNOMED CT 2011_0131)
C2348563 (UMLS CUI 2011AA)
C0521102 (UMLS CUI 2011AA)
78235001 (SNOMED CT 2011_0131)
C1274040 (UMLS CUI 2011AA)
79409006 (SNOMED CT 2011_0131)
C0449295 (UMLS CUI 2011AA)
246175000 (SNOMED CT 2011_0131)
C0023671 (UMLS CUI 2011AA)
LP75025-4 (LOINC Version 232)
10036586 (MedDRA 14.1)
C0006147 (UMLS CUI 2011AA)
10006247 (MedDRA 14.1)
C0032992 (UMLS CUI 2011AA)
169565003 (SNOMED CT 2011_0131)
PART (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C2346570 (UMLS CUI 2011AA)
C0013230 (UMLS CUI 2011AA)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
No comments