ID
12954
Beskrivning
Access II - Trial of Warfarin to Prevent Malfunction of Haemodialysis Catheters; ODM derived from: https://clinicaltrials.gov/show/NCT00157651
Länk
https://clinicaltrials.gov/show/NCT00157651
Nyckelord
Versioner (1)
- 2016-01-07 2016-01-07 -
Rättsinnehavare
CC BY-NC 3.0
Uppladdad den
7 januari 2016
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility End Stage Renal Disease NCT00157651
Eligibility End Stage Renal Disease NCT00157651
- StudyEvent: Eligibility
Beskrivning
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beskrivning
major bleeding
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0019080
Beskrivning
platelet count or coagulopathy
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0005821
- UMLS CUI [2]
- C0005779
Beskrivning
peptic ulcer disease
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0030920
Beskrivning
invasive intervention
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0543467
Beskrivning
warfarin
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0043031
Beskrivning
allergic to, or intolerant of, warfarin
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0043031
Beskrivning
pregnant
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0032961
Beskrivning
woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0009871
Beskrivning
catheter likely needed for 2 weeks or less
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0007430
Beskrivning
patient previously took part in the study
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2348568
Beskrivning
aortic aneurysm
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0003486
Beskrivning
patients nephrologist has refused consent
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0021430
Beskrivning
patient has refused consent
Datatyp
boolean
Alias
- UMLS CUI [1]
- C0021430
Similar models
Eligibility End Stage Renal Disease NCT00157651
- StudyEvent: Eligibility
C0005779 (UMLS CUI [2])
C0043031 (UMLS CUI [1,2])