Eligibility End Stage Renal Disease NCT00157651

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
newly placed double-lumen hemodialysis catheter
Beskrivning

newly placed double-lumen hemodialysis catheter

Datatyp

boolean

Alias
UMLS CUI [1]
C0019004
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
major bleed within last 3 months
Beskrivning

major bleeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0019080
platelet count less than 50 x 10 9/l or current coagulopathy (most recent inr > 1.5, not due to warfarin)
Beskrivning

platelet count or coagulopathy

Datatyp

boolean

Alias
UMLS CUI [1]
C0005821
UMLS CUI [2]
C0005779
active peptic ulcer disease
Beskrivning

peptic ulcer disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0030920
anticipated need for invasive intervention within next 2 weeks
Beskrivning

invasive intervention

Datatyp

boolean

Alias
UMLS CUI [1]
C0543467
taking warfarin for an indication other than access prophylaxis
Beskrivning

warfarin

Datatyp

boolean

Alias
UMLS CUI [1]
C0043031
allergic to, or intolerant of, warfarin
Beskrivning

allergic to, or intolerant of, warfarin

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0043031
pregnant
Beskrivning

pregnant

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
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
catheter likely needed for 2 weeks or less
Beskrivning

catheter likely needed for 2 weeks or less

Datatyp

boolean

Alias
UMLS CUI [1]
C0007430
patient previously took part in the study
Beskrivning

patient previously took part in the study

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
patient has known aortic aneurysm of 6cm or greater
Beskrivning

aortic aneurysm

Datatyp

boolean

Alias
UMLS CUI [1]
C0003486
patients nephrologist has refused consent
Beskrivning

patients nephrologist has refused consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
patient has refused consent
Beskrivning

patient has refused consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility End Stage Renal Disease NCT00157651

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
newly placed double-lumen hemodialysis catheter
Item
newly placed double-lumen hemodialysis catheter
boolean
C0019004 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
major bleeding
Item
major bleed within last 3 months
boolean
C0019080 (UMLS CUI [1])
platelet count or coagulopathy
Item
platelet count less than 50 x 10 9/l or current coagulopathy (most recent inr > 1.5, not due to warfarin)
boolean
C0005821 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
peptic ulcer disease
Item
active peptic ulcer disease
boolean
C0030920 (UMLS CUI [1])
invasive intervention
Item
anticipated need for invasive intervention within next 2 weeks
boolean
C0543467 (UMLS CUI [1])
warfarin
Item
taking warfarin for an indication other than access prophylaxis
boolean
C0043031 (UMLS CUI [1])
allergic to, or intolerant of, warfarin
Item
allergic to, or intolerant of, warfarin
boolean
C0020517 (UMLS CUI [1,1])
C0043031 (UMLS CUI [1,2])
pregnant
Item
pregnant
boolean
C0032961 (UMLS CUI [1])
woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
Item
woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study
boolean
C0009871 (UMLS CUI [1])
catheter likely needed for 2 weeks or less
Item
catheter likely needed for 2 weeks or less
boolean
C0007430 (UMLS CUI [1])
patient previously took part in the study
Item
patient previously took part in the study
boolean
C2348568 (UMLS CUI [1])
aortic aneurysm
Item
patient has known aortic aneurysm of 6cm or greater
boolean
C0003486 (UMLS CUI [1])
patients nephrologist has refused consent
Item
patients nephrologist has refused consent
boolean
C0021430 (UMLS CUI [1])
patient has refused consent
Item
patient has refused consent
boolean
C0021430 (UMLS CUI [1])