ID

12954

Descrizione

Access II - Trial of Warfarin to Prevent Malfunction of Haemodialysis Catheters; ODM derived from: https://clinicaltrials.gov/show/NCT00157651

collegamento

https://clinicaltrials.gov/show/NCT00157651

Keywords

  1. 07/01/16 07/01/16 -
Titolare del copyright

CC BY-NC 3.0

Caricato su

7 gennaio 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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Eligibility End Stage Renal Disease NCT00157651

Eligibility End Stage Renal Disease NCT00157651

Inclusion Criteria
Descrizione

Inclusion Criteria

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

newly placed double-lumen hemodialysis catheter

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0019004
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
major bleed within last 3 months
Descrizione

major bleeding

Tipo di dati

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)
Descrizione

platelet count or coagulopathy

Tipo di dati

boolean

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

peptic ulcer disease

Tipo di dati

boolean

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

invasive intervention

Tipo di dati

boolean

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

warfarin

Tipo di dati

boolean

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

allergic to, or intolerant of, warfarin

Tipo di dati

boolean

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

pregnant

Tipo di dati

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
Descrizione

woman of child-bearing age who has not agreed to use an adequate method of birth control for the duration of the study

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0009871
catheter likely needed for 2 weeks or less
Descrizione

catheter likely needed for 2 weeks or less

Tipo di dati

boolean

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

patient previously took part in the study

Tipo di dati

boolean

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

aortic aneurysm

Tipo di dati

boolean

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

patients nephrologist has refused consent

Tipo di dati

boolean

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

patient has refused consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility End Stage Renal Disease NCT00157651

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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])

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