ID
43316
Description
ODM derived from http://clinicaltrials.gov/show/NCT01369342
Link
http://clinicaltrials.gov/show/NCT01369342
Keywords
Versions (2)
- 4/11/13 4/11/13 - Martin Dugas
- 9/20/21 9/20/21 -
Uploaded on
September 20, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility NCT01369342 Crohn's Disease
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Description
Patients who have had any kind of bowel resection within 6 months
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1514756
- UMLS CUI 2011AA
- CL407060
- UMLS CUI 2011AA
- C1706124
- UMLS CUI 2011AA
- C0741614
- MedDRA 14.1
- 10067878
Description
Are pregnant or planning pregnancy (both men and women) while enrolled in the study or for 20 weeks after receiving study agent
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0549206
- MedDRA 14.1
- 10036586
- UMLS CUI 2011AA
- C0032992
- SNOMED CT 2011_0131
- 169565003
- UMLS CUI 2011AA
- C0025266
- SNOMED CT 2011_0131
- 339947000
- UMLS CUI 2011AA
- C0043210
- SNOMED CT 2011_0131
- 224526002
Description
Patients who have received infliximab, adalimumab or certolizumab pegol < = 8 weeks before the first administration of study drug
Data type
boolean
Alias
- UMLS CUI 2011AA
- C1514756
- UMLS CUI 2011AA
- C0666743
- SNOMED CT 2011_0131
- 386891004
- LOINC Version 232
- MTHU018219
- UMLS CUI 2011AA
- C1122087
- SNOMED CT 2011_0131
- 407317001
- UMLS CUI 2011AA
- C1172157
- SNOMED CT 2011_0131
- 430307008
- UMLS CUI 2011AA
- C0332152
- SNOMED CT 2011_0131
- 288556008
- UMLS CUI 2011AA
- C1533734
- SNOMED CT 2011_0131
- 416118004
- UMLS CUI 2011AA
- C0304229
- SNOMED CT 2011_0131
- 902003
Description
Patients with certain complications of Crohn's disease that would make it hard to assess response to study drug
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0009566
- SNOMED CT 2011_0131
- 116223007
- LOINC Version 232
- MTHU008883
- UMLS CUI 2011AA
- C0010346
- SNOMED CT 2011_0131
- 34000006
- MedDRA 14.1
- 10011401
- ICD-10-CM Version 2010
- K50.9
- UMLS CUI 2011AA
- C1299586
- SNOMED CT 2011_0131
- 52925006
- UMLS CUI 2011AA
- C1516048
- UMLS CUI 2011AA
- C0871261
- UMLS CUI 2011AA
- C0304229
- SNOMED CT 2011_0131
- 902003
Description
Patients with a history of or ongoing chronic or recurrent infectious disease
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0151317
- SNOMED CT 2011_0131
- 177010002
- UMLS CUI 2011AA
- CL429630
- UMLS CUI 2011AA
- C0009450
- SNOMED CT 2011_0131
- 40733004
- MedDRA 14.1
- 10021881
- LOINC Version 232
- MTHU034915
- ICD-9-CM Version 2011
- 136.9
Description
Patients who have previously received a biologic agent targeting IL-12 or IL-23, including but not limited to ustekinumab (CNTO 1275) or briakinumab (ABT-874)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0205156
- SNOMED CT 2011_0131
- 9130008
- UMLS CUI 2011AA
- C1514756
- UMLS CUI 2011AA
- C0005515
- UMLS CUI 2011AA
- C1521840
- UMLS CUI 2011AA
- C0123759
- SNOMED CT 2011_0131
- 6411000
- LOINC Version 232
- MTHU003527
- UMLS CUI 2011AA
- C0963088
- UMLS CUI 2011AA
- C0332257
- SNOMED CT 2011_0131
- 55919000
- UMLS CUI 2011AA
- C1608841
- SNOMED CT 2011_0131
- 443644001
- UMLS CUI 2011AA
- C2744325
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- StudyEvent: Eligibility
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