ID
43352
Description
ODM derived from http://clinicaltrials.gov/show/NCT00241514
Link
http://clinicaltrials.gov/show/NCT00241514
Keywords
Versions (2)
- 4/14/14 4/14/14 - Julian Varghese
- 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 NCT00241514 GERD
Eligibility
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI 2011AA
- CL425201
Description
Discontinuation from study SH-NEN-0001
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0457454
- SNOMED CT 2011_0131
- 278308006
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
Description
Pain, discomfort or burning in the upper abdomen precipitated by exercise or relieved by defecation.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0030193
- SNOMED CT 2011_0131
- 22253000
- MedDRA 14.1
- 10033371
- LOINC Version 232
- MTHU029813
- ICD-10-CM Version 2010
- R52
- ICD-9-CM Version 2011
- 338-338.9
- CTCAE 1105E
- E11167
- UMLS CUI 2011AA
- CL355048
- SNOMED CT 2011_0131
- 247347003
- UMLS CUI 2011AA
- C0085624
- SNOMED CT 2011_0131
- 90673000
- MedDRA 14.1
- 10006784
- UMLS CUI 2011AA
- C2937240
- SNOMED CT 2011_0131
- 80581009
- UMLS CUI 2011AA
- C1444748
- SNOMED CT 2011_0131
- 410658008
- UMLS CUI 2011AA
- C0015259
- SNOMED CT 2011_0131
- 256235009
- MedDRA 14.1
- 10015634
- UMLS CUI 2011AA
- C0332303
- SNOMED CT 2011_0131
- 1241001
- UMLS CUI 2011AA
- C0011135
- SNOMED CT 2011_0131
- 39211005
Description
Pain, discomfort or burning in the upper abdomen not associated with the use of NSAIDs, including COX-2 selective NSAIDs.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0030193
- SNOMED CT 2011_0131
- 22253000
- MedDRA 14.1
- 10033371
- LOINC Version 232
- MTHU029813
- ICD-10-CM Version 2010
- R52
- ICD-9-CM Version 2011
- 338-338.9
- CTCAE 1105E
- E11167
- UMLS CUI 2011AA
- CL355048
- SNOMED CT 2011_0131
- 247347003
- UMLS CUI 2011AA
- C0085624
- SNOMED CT 2011_0131
- 90673000
- MedDRA 14.1
- 10006784
- UMLS CUI 2011AA
- C2937240
- SNOMED CT 2011_0131
- 80581009
- UMLS CUI 2011AA
- C1518422
- UMLS CUI 2011AA
- C0332281
- SNOMED CT 2011_0131
- 47429007
- UMLS CUI 2011AA
- C1524063
- SNOMED CT 2011_0131
- 260676000
- UMLS CUI 2011AA
- C0003211
- SNOMED CT 2011_0131
- 16403005
- UMLS CUI 2011AA
- C0332257
- SNOMED CT 2011_0131
- 55919000
- UMLS CUI 2011AA
- C1257954
- SNOMED CT 2011_0131
- 387050005
Description
Pregnancy or lactation. Women of childbearing potential must maintain effective contraception during the study period as judged by the investigator.
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0032961
- SNOMED CT 2011_0131
- 289908002
- MedDRA 14.1
- 10036556
- LOINC Version 232
- MTHU035048
- UMLS CUI 2011AA
- C0006147
- MedDRA 14.1
- 10006247
- UMLS CUI 2011AA
- C0043210
- SNOMED CT 2011_0131
- 224526002
- UMLS CUI 2011AA
- C1148523
- UMLS CUI 2011AA
- C0237399
- UMLS CUI 2011AA
- C0024501
- UMLS CUI 2011AA
- C1704419
- SNOMED CT 2011_0131
- 254648000
- UMLS CUI 2011AA
- C0700589
- SNOMED CT 2011_0131
- 146680009
- MedDRA 14.1
- 10010808
- UMLS CUI 2011AA
- C0347984
- SNOMED CT 2011_0131
- 371881003
- UMLS CUI 2011AA
- C0008976
- SNOMED CT 2011_0131
- 110465008
- UMLS CUI 2011AA
- C1948053
- UMLS CUI 2011AA
- C0022423
- SNOMED CT 2011_0131
- 61254005
- UMLS CUI 2011AA
- CL102947
Description
Need for continuous concomitant therapy with: (Anticoagulants, Corticosteroids at doses higher than explained under inclusion criterion)
Data type
boolean
Alias
- UMLS CUI 2011AA
- C0686904
- SNOMED CT 2011_0131
- 103325001
- UMLS CUI 2011AA
- C0549178
- UMLS CUI 2011AA
- C1707479
- UMLS CUI 2011AA
- C0003280
- SNOMED CT 2011_0131
- 372862008
- UMLS CUI 2011AA
- C0001617
- SNOMED CT 2011_0131
- 79440004
- UMLS CUI 2011AA
- C0178602
- SNOMED CT 2011_0131
- 260911001
- UMLS CUI 2011AA
- C0444956
- SNOMED CT 2011_0131
- 261829003
- UMLS CUI 2011AA
- C0681841
- LOINC Version 232
- MTHU013812
- UMLS CUI 2011AA
- CL425202
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