ID
5048
Description
ODM derived from http://clinicaltrials.gov/show/NCT00932724
Lien
http://clinicaltrials.gov/show/NCT00932724
Mots-clés
Versions (4)
- 09/12/2013 09/12/2013 - Martin Dugas
- 17/04/2014 17/04/2014 - Julian Varghese
- 15/03/2021 15/03/2021 - Dr. rer. medic Philipp Neuhaus
- 20/09/2021 20/09/2021 -
Téléchargé le
17 avril 2014
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility NCT00932724 Metastatic Colorectal Cancer
Eligibility
- StudyEvent: Eligibility
Description
Ausschlusskriterien
Alias
- UMLS CUI 2011AA
- CL425201
Description
Evidence of any other malignant disease (with the exception of tumors operatively cured >= 5 years prior to the trial)
Type de données
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
Description
Known brain metastases
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0220650
- MedDRA 14.1
- 10006128
Description
Uncontrolled pleural effusions
Type de données
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
Description
Interstitial pneumonitis or pulmonary fibrosis
Type de données
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
Description
Severe/ unstable systemic disease or infection and circumstances not permitting trial participation (e.g., alcoholism or substance abuse)
Type de données
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
Description
Unstable cardiac disease in the last 6 months
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C0443343
- SNOMED CT 2011_0131
- 263922001
- UMLS CUI 2011AA
- C0018799
- SNOMED CT 2011_0131
- 56265001
- MedDRA 14.1
- 10061024
Description
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
Type de données
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
Description
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
Type de données
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
Description
Any history or evidence of pulmonary embolism or thrombophlebitis (including deep vein thrombosis) requiring anticoagulant therapy (e.g., marcumar or heparin)
Type de données
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
Description
History of hypersensitivity to mistletoe
Type de données
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
Description
History of primary immunodeficiency
Type de données
boolean
Alias
- UMLS CUI 2011AA
- CL421546
- SNOMED CT 2011_0131
- 392521001
- UMLS CUI 2011AA
- C0398686
- SNOMED CT 2011_0131
- 58606001
- MedDRA 14.1
- 10064859
Description
Known human immunodeficiency virus (HIV) or known active viral hepatic infections
Type de données
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
Description
Prior treatment with CY-503
Type de données
boolean
Alias
- UMLS CUI 2011AA
- C1514463
- UMLS CUI 2011AA
- C0150312
- SNOMED CT 2011_0131
- 52101004
- UMLS CUI 2011AA
- C0013230
Description
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
Type de données
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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Eligibility
- StudyEvent: Eligibility
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146680009 (SNOMED CT 2011_0131)
10010808 (MedDRA 14.1)
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248152002 (SNOMED CT 2011_0131)
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C0232973 (UMLS CUI 2011AA)
60001007 (SNOMED CT 2011_0131)
C2826207 (UMLS CUI 2011AA)
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10047939 (MedDRA 14.1)
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10037032 (MedDRA 14.1)
R80 (ICD-10-CM Version 2010)
791.0 (ICD-9-CM Version 2011)
E13008 (CTCAE 1105E)
C0456209 (UMLS CUI 2011AA)
276833005 (SNOMED CT 2011_0131)
C0430371 (UMLS CUI 2011AA)
271346009 (SNOMED CT 2011_0131)
CL415097 (UMLS CUI 2011AA)
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51615001 (SNOMED CT 2011_0131)
10037383 (MedDRA 14.1)
J84.1 (ICD-10-CM Version 2010)
E13527 (CTCAE 1105E)
24484000 (SNOMED CT 2011_0131)
C0443343 (UMLS CUI 2011AA)
263922001 (SNOMED CT 2011_0131)
C0442893 (UMLS CUI 2011AA)
56019007, 264578000 (SNOMED CT 2011_0131)
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257551009 (SNOMED CT 2011_0131)
10021789 (MedDRA 14.1)
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10044390 (MedDRA 14.1)
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G45.9 (ICD-10-CM Version 2010)
435.9 (ICD-9-CM Version 2011)
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59282003 (SNOMED CT 2011_0131)
10037377 (MedDRA 14.1)
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10043570 (MedDRA 14.1)
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128053003 (SNOMED CT 2011_0131)
10051055 (MedDRA 14.1)
I82.40 (ICD-10-CM Version 2010)
C1514873 (UMLS CUI 2011AA)
C0150457 (UMLS CUI 2011AA)
182764009 (SNOMED CT 2011_0131)
10053468 (MedDRA 14.1)
C0918269 (UMLS CUI 2011AA)
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)
T78.40 (ICD-10-CM Version 2010)
C0042785 (UMLS CUI 2011AA)
43601004 (SNOMED CT 2011_0131)
392521001 (SNOMED CT 2011_0131)
C0398686 (UMLS CUI 2011AA)
58606001 (SNOMED CT 2011_0131)
10064859 (MedDRA 14.1)
19030005 (SNOMED CT 2011_0131)
C0205177 (UMLS CUI 2011AA)
55561003 (SNOMED CT 2011_0131)
C0042721 (UMLS CUI 2011AA)
3738000 (SNOMED CT 2011_0131)
10019799 (MedDRA 14.1)
MTHU020837 (LOINC Version 232)
B19 (ICD-10-CM Version 2010)
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E11410 (CTCAE 1105E)
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52101004 (SNOMED CT 2011_0131)
C0013230 (UMLS CUI 2011AA)
MEDCCAT (HL7 V3 2006_05)
C0423895 (UMLS CUI 2011AA)
247571009 (SNOMED CT 2011_0131)
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2403008 (SNOMED CT 2011_0131)
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66214007 (SNOMED CT 2011_0131)
10066169 (MedDRA 14.1)
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116154003 (SNOMED CT 2011_0131)
C1299582 (UMLS CUI 2011AA)
371151008 (SNOMED CT 2011_0131)
C1554962 (UMLS CUI 2011AA)
C (HL7 V3 2006_05)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C1519316 (UMLS CUI 2011AA)
C0021430 (UMLS CUI 2011AA)