ID

4763

Beschrijving

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

Link

http://clinicaltrials.gov/show/NCT00824083

Trefwoorden

  1. 25-07-13 25-07-13 - Martin Dugas
  2. 27-03-14 27-03-14 - Martin Dugas
Geüploaded op

27 maart 2014

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility DRKS00003588 NCT00824083 Sarcoma, Ewing's

Eligibility Ewing Sarcoma NCT00824083

Einschlusskriterien
Beschrijving

Einschlusskriterien

Alias
UMLS CUI 2011AA
CL425202
Alter 6 bis 60 Jahre
Beschrijving

age

Datatype

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)
Beschrijving

Trial participant (Ewing trials GPOH)

Datatype

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
Ausschlusskriterien
Beschrijving

Ausschlusskriterien

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

no complete remission (CR)

Datatype

boolean

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

Paralysis

Datatype

boolean

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

Time after diagnosis

Datatype

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

Similar models

Eligibility Ewing Sarcoma NCT00824083

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Einschlusskriterien
CL425202 (UMLS CUI 2011AA)
age
Item
Alter 6 bis 60 Jahre
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
Ausschlusskriterien
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
<5y 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)

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