ID
12954
Beschrijving
Access II - Trial of Warfarin to Prevent Malfunction of Haemodialysis Catheters; ODM derived from: https://clinicaltrials.gov/show/NCT00157651
Link
https://clinicaltrials.gov/show/NCT00157651
Trefwoorden
Versies (1)
- 07-01-16 07-01-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
7 januari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility End Stage Renal Disease NCT00157651
Eligibility End Stage Renal Disease NCT00157651
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschrijving
major bleeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0019080
Beschrijving
platelet count or coagulopathy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0005821
- UMLS CUI [2]
- C0005779
Beschrijving
peptic ulcer disease
Datatype
boolean
Alias
- UMLS CUI [1]
- C0030920
Beschrijving
invasive intervention
Datatype
boolean
Alias
- UMLS CUI [1]
- C0543467
Beschrijving
warfarin
Datatype
boolean
Alias
- UMLS CUI [1]
- C0043031
Beschrijving
allergic to, or intolerant of, warfarin
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0043031
Beschrijving
pregnant
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
Beschrijving
woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009871
Beschrijving
catheter likely needed for 2 weeks or less
Datatype
boolean
Alias
- UMLS CUI [1]
- C0007430
Beschrijving
patient previously took part in the study
Datatype
boolean
Alias
- UMLS CUI [1]
- C2348568
Beschrijving
aortic aneurysm
Datatype
boolean
Alias
- UMLS CUI [1]
- C0003486
Beschrijving
patients nephrologist has refused consent
Datatype
boolean
Alias
- UMLS CUI [1]
- C0021430
Beschrijving
patient has refused consent
Datatype
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])