ID
42025
Beschrijving
ODM derived from http://clinicaltrials.gov/show/NCT00932724
Link
http://clinicaltrials.gov/show/NCT00932724
Trefwoorden
Versies (4)
- 09-12-13 09-12-13 - Martin Dugas
- 17-04-14 17-04-14 - Julian Varghese
- 15-03-21 15-03-21 - Dr. rer. medic Philipp Neuhaus
- 20-09-21 20-09-21 -
Geüploaded op
15 maart 2021
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility NCT00932724 Metastatic Colorectal Cancer
Eligibility
- StudyEvent: Eligibility
Beschrijving
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Beschrijving
Evidence of any other malignant disease (with the exception of tumors operatively cured >= 5 years prior to the trial)
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205394
- SNOMED CT 2011_0131
- 74964007
- UMLS CUI 2011AA
- C0006826
- SNOMED CT 2011_0131
- 363346000
- MedDRA 14.1
- 10028997
- LOINC Version 232
- MTHU010328
- ICD-10-CM Version 2010
- C00-C96
- UMLS CUI 2011AA
- C1554961
- HL7 V3 2006_05
- E
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C0543467
- SNOMED CT 2011_0131
- 83578000
- MedDRA 14.1
- 10051332
- LOINC Version 232
- MTHU000079
- UMLS CUI 2011AA
- C1880198
Beschrijving
Known brain metastases
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0220650
- MedDRA 14.1
- 10006128
Beschrijving
Uncontrolled pleural effusions
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205318
- SNOMED CT 2011_0131
- 19032002
- UMLS CUI 2011AA
- C0032227
- SNOMED CT 2011_0131
- 60046008
- MedDRA 14.1
- 10035598
- ICD-10-CM Version 2010
- J90
- ICD-9-CM Version 2011
- 511.9
- CTCAE 1105E
- E13486
Beschrijving
Interstitial pneumonitis or pulmonary fibrosis
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0206061
- SNOMED CT 2011_0131
- 64667001
- MedDRA 14.1
- 10022618
- ICD-10-CM Version 2010
- J84.9
- UMLS CUI 2011AA
- C0034069
- SNOMED CT 2011_0131
- 51615001
- MedDRA 14.1
- 10037383
- ICD-10-CM Version 2010
- J84.1
- CTCAE 1105E
- E13527
Beschrijving
Severe/ unstable systemic disease or infection and circumstances not permitting trial participation (e.g., alcoholism or substance abuse)
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0205082
- SNOMED CT 2011_0131
- 24484000
- UMLS CUI 2011AA
- C0443343
- SNOMED CT 2011_0131
- 263922001
- UMLS CUI 2011AA
- C0442893
- SNOMED CT 2011_0131
- 56019007, 264578000
- UMLS CUI 2011AA
- C0021311
- SNOMED CT 2011_0131
- 257551009
- MedDRA 14.1
- 10021789
- UMLS CUI 2011AA
- C0683578
- UMLS CUI 2011AA
- C1554075
- HL7 V3 2006_05
- NP
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
- UMLS CUI 2011AA
- C0679823
- HL7 V3 2006_05
- PART
- UMLS CUI 2011AA
- C0001973
- SNOMED CT 2011_0131
- 284591009
- MedDRA 14.1
- 10001639
- ICD-10-CM Version 2010
- F10.2
- ICD-9-CM Version 2011
- 305.01
- UMLS CUI 2011AA
- C0740858
- SNOMED CT 2011_0131
- 66214007
- MedDRA 14.1
- 10066169
- LOINC Version 232
- MTHU019364
Beschrijving
Unstable cardiac disease in the last 6 months
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0443343
- SNOMED CT 2011_0131
- 263922001
- UMLS CUI 2011AA
- C0018799
- SNOMED CT 2011_0131
- 56265001
- MedDRA 14.1
- 10061024
Beschrijving
Use of conventional mistletoe preparations, any immunostimulating substances and/or monoclonal antibodies within four weeks prior to and during the trial - ongoing therapy with steroids is permitted if the dose is not > 20 mg of prednisone-equivalent at the time of inclusion and during this clinical trial
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C1166209
- UMLS CUI 2011AA
- CL414476
- UMLS CUI 2011AA
- C0003250
- SNOMED CT 2011_0131
- 49616005
- UMLS CUI 2011AA
- C0521104
- SNOMED CT 2011_0131
- 75554001
- UMLS CUI 2011AA
- C1708745
- UMLS CUI 2011AA
- C0149783
- SNOMED CT 2011_0131
- 297279009
- MedDRA 14.1
- 10062117
Beschrijving
Any evidence or history (elicited by the investigator) of symptomatic cerebrovascular events (i.e., stroke or transient ischemic attack) within 6 months prior to randomization
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0231220
- SNOMED CT 2011_0131
- 264931009
- UMLS CUI 2011AA
- C1880018
- UMLS CUI 2011AA
- C0441471
- SNOMED CT 2011_0131
- 272379006
- LOINC Version 232
- MTHU019184
- UMLS CUI 2011AA
- C0038454
- SNOMED CT 2011_0131
- 230690007
- MedDRA 14.1
- 10042244
- ICD-10-CM Version 2010
- I63.9
- CTCAE 1105E
- E12826
- UMLS CUI 2011AA
- C0007787
- SNOMED CT 2011_0131
- 266257000
- MedDRA 14.1
- 10044390
- LOINC Version 232
- MTHU020810
- ICD-10-CM Version 2010
- G45.9
- ICD-9-CM Version 2011
- 435.9
- CTCAE 1105E
- E12834
Beschrijving
Any history or evidence of pulmonary embolism or thrombophlebitis (including deep vein thrombosis) requiring anticoagulant therapy (e.g., marcumar or heparin)
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0034065
- SNOMED CT 2011_0131
- 59282003
- MedDRA 14.1
- 10037377
- ICD-10-CM Version 2010
- I26
- ICD-9-CM Version 2011
- 415.1
- UMLS CUI 2011AA
- C0040046
- SNOMED CT 2011_0131
- 64156001
- MedDRA 14.1
- 10043570
- UMLS CUI 2011AA
- C0149871
- SNOMED CT 2011_0131
- 128053003
- MedDRA 14.1
- 10051055
- ICD-10-CM Version 2010
- I82.40
- UMLS CUI 2011AA
- C1514873
- UMLS CUI 2011AA
- C0150457
- SNOMED CT 2011_0131
- 182764009
- MedDRA 14.1
- 10053468
- UMLS CUI 2011AA
- C0918269
- UMLS CUI 2011AA
- C0019134
- SNOMED CT 2011_0131
- 372877000
- LOINC Version 232
- MTHU003766
Beschrijving
History of hypersensitivity to mistletoe
Datatype
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0020517
- SNOMED CT 2011_0131
- 418634005
- ICD-10-CM Version 2010
- T78.40
- UMLS CUI 2011AA
- C0042785
- SNOMED CT 2011_0131
- 43601004
Beschrijving
History of primary immunodeficiency
Datatype
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0398686
- SNOMED CT 2011_0131
- 58606001
- MedDRA 14.1
- 10064859
Beschrijving
Known human immunodeficiency virus (HIV) or known active viral hepatic infections
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C0019682
- SNOMED CT 2011_0131
- 19030005
- UMLS CUI 2011AA
- C0205177
- SNOMED CT 2011_0131
- 55561003
- UMLS CUI 2011AA
- C0042721
- SNOMED CT 2011_0131
- 3738000
- MedDRA 14.1
- 10019799
- LOINC Version 232
- MTHU020837
- ICD-10-CM Version 2010
- B19
- ICD-9-CM Version 2011
- 070
- CTCAE 1105E
- E11410
Beschrijving
Prior treatment with CY-503
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C1514463
- UMLS CUI 2011AA
- C0150312
- SNOMED CT 2011_0131
- 52101004
- UMLS CUI 2011AA
- C0013230
Beschrijving
A general medical or psychological condition or behaviour, including substance dependence or abuse that, in the opinion of the investigator, might not permit the patient to complete the trial or sign the informed consent
Datatype
boolean
Alias
- UMLS CUI 2011AA
- C1699700
- HL7 V3 2006_05
- MEDCCAT
- UMLS CUI 2011AA
- C0423895
- SNOMED CT 2011_0131
- 247571009
- UMLS CUI 2011AA
- C0038580
- SNOMED CT 2011_0131
- 2403008
- UMLS CUI 2011AA
- C0740858
- SNOMED CT 2011_0131
- 66214007
- MedDRA 14.1
- 10066169
- LOINC Version 232
- MTHU019364
- UMLS CUI 2011AA
- C0030705
- SNOMED CT 2011_0131
- 116154003
- UMLS CUI 2011AA
- C1299582
- SNOMED CT 2011_0131
- 371151008
- UMLS CUI 2011AA
- C1554962
- HL7 V3 2006_05
- C
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
- UMLS CUI 2011AA
- C1519316
- UMLS CUI 2011AA
- C0021430
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24484000 (SNOMED CT 2011_0131)
C0443343 (UMLS CUI 2011AA)
263922001 (SNOMED CT 2011_0131)
C0442893 (UMLS CUI 2011AA)
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257551009 (SNOMED CT 2011_0131)
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C0019134 (UMLS CUI 2011AA)
372877000 (SNOMED CT 2011_0131)
MTHU003766 (LOINC Version 232)
392521001 (SNOMED CT 2011_0131)
C0020517 (UMLS CUI 2011AA)
418634005 (SNOMED CT 2011_0131)
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C0042785 (UMLS CUI 2011AA)
43601004 (SNOMED CT 2011_0131)
392521001 (SNOMED CT 2011_0131)
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55561003 (SNOMED CT 2011_0131)
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10019799 (MedDRA 14.1)
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