ID
27590
Beschrijving
PeriOperative ISchemic Evaluation-2 Pilot; ODM derived from: https://clinicaltrials.gov/show/NCT00860925
Link
https://clinicaltrials.gov/show/NCT00860925
Trefwoorden
Versies (2)
- 21-11-17 21-11-17 -
- 27-09-21 27-09-21 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
21 november 2017
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT00860925
Eligibility Cardiovascular Disease NCT00860925
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
Aspirin
Datatype
boolean
Alias
- UMLS CUI [1]
- C0004057
Beschrijving
Aspirin allergy | Clonidine allergy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0004058
- UMLS CUI [2]
- C0570975
Beschrijving
Systolic Pressure
Datatype
boolean
Alias
- UMLS CUI [1]
- C0871470
Beschrijving
Heart rate
Datatype
boolean
Alias
- UMLS CUI [1]
- C0018810
Beschrijving
Second degree atrioventricular block | Complete atrioventricular block | Artificial cardiac pacemaker Absent
Datatype
boolean
Alias
- UMLS CUI [1]
- C0264906
- UMLS CUI [2]
- C0151517
- UMLS CUI [3,1]
- C0030163
- UMLS CUI [3,2]
- C0332197
Beschrijving
Peptic Ulcer
Datatype
boolean
Alias
- UMLS CUI [1]
- C0030920
Beschrijving
Bare metal stent
Datatype
boolean
Alias
- UMLS CUI [1]
- C2825200
Beschrijving
Drug-Eluting Stents
Datatype
boolean
Alias
- UMLS CUI [1]
- C1322815
Beschrijving
Alpha 2 agonist | alpha-methyldopa | Reserpine | clopidogrel | Ticlopidine
Datatype
boolean
Alias
- UMLS CUI [1]
- C1268904
- UMLS CUI [2]
- C0025741
- UMLS CUI [3]
- C0035179
- UMLS CUI [4]
- C0070166
- UMLS CUI [5]
- C0040207
Beschrijving
Intracranial surgery | Carotid Endarterectomy | Operation on retina
Datatype
boolean
Alias
- UMLS CUI [1]
- C0745377
- UMLS CUI [2]
- C0014099
- UMLS CUI [3]
- C0197770
Beschrijving
Study Subject Participation Status Surgeon Unwilling | Clonidine Trial perioperative | Aspirin Trial perioperative
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C0582175
- UMLS CUI [1,3]
- C0558080
- UMLS CUI [2,1]
- C0009014
- UMLS CUI [2,2]
- C0008976
- UMLS CUI [2,3]
- C1518988
- UMLS CUI [3,1]
- C0004057
- UMLS CUI [3,2]
- C0008976
- UMLS CUI [3,3]
- C1518988
Beschrijving
Enrollment Clinical Trial Specified
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1516879
- UMLS CUI [1,2]
- C0008976
- UMLS CUI [1,3]
- C0205369
Beschrijving
Informed Consent Unable | Informed Consent Refused
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C1299582
- UMLS CUI [2,1]
- C0021430
- UMLS CUI [2,2]
- C1705116
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Eligibility Cardiovascular Disease NCT00860925
- StudyEvent: Eligibility
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C0018821 (UMLS CUI [2,2])
C0439583 (UMLS CUI [1,2])
C0032790 (UMLS CUI [1,3])
C1517001 (UMLS CUI [1,4])
C0543467 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0018821 (UMLS CUI [3,2])
C0205164 (UMLS CUI [1,2])
C0042381 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0684204 (UMLS CUI [3,2])
C1705847 (UMLS CUI [4,1])
C0149807 (UMLS CUI [4,2])
C1705847 (UMLS CUI [5,1])
C0014099 (UMLS CUI [5,2])
C0243161 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0543467 (UMLS CUI [2,1])
C0442120 (UMLS CUI [2,2])
C0524832 (UMLS CUI [3])
C1136201 (UMLS CUI [4])
C0359086 (UMLS CUI [2])
C0021641 (UMLS CUI [3])
C0570975 (UMLS CUI [2])
C0151517 (UMLS CUI [2])
C0030163 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0025741 (UMLS CUI [2])
C0035179 (UMLS CUI [3])
C0070166 (UMLS CUI [4])
C0040207 (UMLS CUI [5])
C0014099 (UMLS CUI [2])
C0197770 (UMLS CUI [3])
C0582175 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,3])
C0009014 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C1518988 (UMLS CUI [2,3])
C0004057 (UMLS CUI [3,1])
C0008976 (UMLS CUI [3,2])
C1518988 (UMLS CUI [3,3])
C0008976 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])