Information:
Fel:
ID
22529
Beskrivning
ODM derived from http://clinicaltrials.gov/show/NCT00251966
Länk
http://clinicaltrials.gov/show/NCT00251966
Nyckelord
Versioner (2)
- 2012-02-21 2012-02-21 -
- 2017-06-06 2017-06-06 - Martin Dugas
Uppladdad den
6 juni 2017
DOI
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Licens
Creative Commons BY 4.0
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ASTERIX: Low Dose ASA and Nexium
Eligibility
- StudyEvent: Eligibility
Beskrivning
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Similar models
Eligibility
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Age
Item
Age >= 60 years
boolean
C0001779 (UMLS CUI [1])
Low Dose ASA
Item
A clinical diagnosis of a condition (cardiovascular and/or cerebrovascular protection or other reasons) that requires daily intake of low-dose ASA, 75-325 mg, and is expected to continue for the duration of the study (daily is defined as at least 5 days per week)
boolean
C0721444 (UMLS CUI [1])
No gastric or duodenal ulcer
Item
No gastric and/or duodenal ulcer at the baseline endoscopy
boolean
C3843755 (UMLS CUI [1,1])
C3640974 (UMLS CUI [1,2])
C3640974 (UMLS CUI [1,2])
H. pylori negative
Item
H. pylori negative by serology test at screening
boolean
C1167693 (UMLS CUI [1])
Upper GI symptoms
Item
Upper GI symptoms
boolean
C3645762 (UMLS CUI [1])
Erosive oesophagitis
Item
Erosive oesophagitis
boolean
C0267055 (UMLS CUI [1])
Malignancy
Item
Malignancy
boolean
C0006826 (UMLS CUI [1])