ID

4763

Beskrivning

Functional and Clinical Long-Term Outcome of Ewing Sarcoma Treatment see http://clinicaltrials.gov/show/NCT00824083

Länk

http://clinicaltrials.gov/show/NCT00824083

Nyckelord

Versioner (2)
  1. 2013-07-25 2013-07-25 - Martin Dugas
  2. 2014-03-27 2014-03-27 - Martin Dugas
Uppladdad den

27 mars 2014

DOI

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Licens

Creative Commons BY 4.0
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Eligibility DRKS00003588 NCT00824083 Sarcoma, Ewing's

Tysk Engelsk

Eligibility Ewing Sarcoma NCT00824083

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI 2011AA
CL425202
age 6 Years to 60 Years
Beskrivning

age

Datatyp

boolean

Alias
SNOMED CT 2011_0131
397669002
UMLS CUI-1
C0001779
CESS81/CESS86/EICESS92/EURO-E.W.I.N.G.99 trials participants of the German Society of Pediatric Hematology and Oncology (GPOH)
Beskrivning

Trial participant (Ewing trials GPOH)

Datatyp

boolean

Alias
SNOMED CT 2011_0131
414152003
HL7 V3 2006_05
2108-9
SNOMED CT 2011_0131
76909002
MedDRA 14.1
10015560
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
SNOMED CT 2011_0131
110465008
SNOMED CT 2011_0131
418652005
SNOMED CT 2011_0131
418002000
UMLS CUI-1
C0553580
UMLS CUI-2
C0008976
UMLS CUI-3
C0679646
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
no complete remission (CR)
Beskrivning

no complete remission (CR)

Datatyp

boolean

Alias
UMLS CUI 2011AA
C1518422
UMLS CUI 2011AA
C0677874
SNOMED CT 2011_0131
103338009
any kind of paralysis
Beskrivning

Paralysis

Datatyp

boolean

Alias
SNOMED CT 2011_0131
44695005
MedDRA 14.1
10033799
ICD-9-CM Version 2011
344.9
UMLS CUI-1
C0522224
<5years after diagnosis
Beskrivning

Time after diagnosis

Datatyp

boolean

Alias
SNOMED CT 2011_0131
276139006
HL7 V3 2006_05
LT
SNOMED CT 2011_0131
34001005
SNOMED CT 2011_0131
258707000
HL7 V3 2006_05
Y
SNOMED CT 2011_0131
237679004
SNOMED CT 2011_0131
439401001
LOINC Version 232
MTHU008876
UMLS CUI-1
C0231290
UMLS CUI-2
C0011900
Tillbaka till toppen

Similar models

Eligibility Ewing Sarcoma NCT00824083

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion Criteria
CL425202 (UMLS CUI 2011AA)
age
Item
age 6 Years to 60 Years
boolean
397669002 (SNOMED CT 2011_0131)
C0001779 (UMLS CUI-1)
Trial participant (Ewing trials GPOH)
Item
CESS81/CESS86/EICESS92/EURO-E.W.I.N.G.99 trials participants of the German Society of Pediatric Hematology and Oncology (GPOH)
boolean
414152003 (SNOMED CT 2011_0131)
2108-9 (HL7 V3 2006_05)
76909002 (SNOMED CT 2011_0131)
10015560 (MedDRA 14.1)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
110465008 (SNOMED CT 2011_0131)
418652005 (SNOMED CT 2011_0131)
418002000 (SNOMED CT 2011_0131)
C0553580 (UMLS CUI-1)
C0008976 (UMLS CUI-2)
C0679646 (UMLS CUI-3)
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
no complete remission (CR)
Item
no complete remission (CR)
boolean
C1518422 (UMLS CUI 2011AA)
C0677874 (UMLS CUI 2011AA)
103338009 (SNOMED CT 2011_0131)
Paralysis
Item
any kind of paralysis
boolean
44695005 (SNOMED CT 2011_0131)
10033799 (MedDRA 14.1)
344.9 (ICD-9-CM Version 2011)
C0522224 (UMLS CUI-1)
Time after diagnosis
Item
<5years after diagnosis
boolean
276139006 (SNOMED CT 2011_0131)
LT (HL7 V3 2006_05)
34001005 (SNOMED CT 2011_0131)
258707000 (SNOMED CT 2011_0131)
Y (HL7 V3 2006_05)
237679004 (SNOMED CT 2011_0131)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0231290 (UMLS CUI-1)
C0011900 (UMLS CUI-2)
Tillbaka till toppen 

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