ID
4447
Beschrijving
ODM derived from http://clinicaltrials.gov/show/NCT00700141
Link
http://clinicaltrials.gov/show/NCT00700141
Trefwoorden
Versies (1)
- 09-12-13 09-12-13 - Martin Dugas
Geüploaded op
9 december 2013
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility NCT00700141 Hemorrhage
Eligibility
- StudyEvent: Eligibility
Beschrijving
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Beschrijving
Contraindications, such as hypersensitivity to the active pharmaceutical ingredient or to another ingredient
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C1301624
- SNOMED CT 2011_0131
- 397745006
- UMLS CUI 2011AA
- C0020517
- SNOMED CT 2011_0131
- 418634005
- ICD-10-CM Version 2010
- T78.40
- UMLS CUI 2011AA
- C0031336
- UMLS CUI 2011AA
- C1372955
- HL7 V3 2006_05
- ACTI
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- CL414967
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Eligibility
- StudyEvent: Eligibility
397669002 (SNOMED CT 2011_0131)
50960005 (SNOMED CT 2011_0131)
10055798 (MedDRA 14.1)
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C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
24443003 (SNOMED CT 2011_0131)
10043777 (MedDRA 14.1)
41005 (ICD-9-CM Version 2011)
C0193790 (UMLS CUI 2011AA)
30956003 (SNOMED CT 2011_0131)
10043776 (MedDRA 14.1)
397745006 (SNOMED CT 2011_0131)
C0020517 (UMLS CUI 2011AA)
418634005 (SNOMED CT 2011_0131)
T78.40 (ICD-10-CM Version 2010)
C0031336 (UMLS CUI 2011AA)
C1372955 (UMLS CUI 2011AA)
ACTI (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
CL414967 (UMLS CUI 2011AA)