ID

12954

Description

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

Keywords

  1. 1/7/16 1/7/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 7, 2016

DOI

To request one please log in.

License

Creative Commons BY-NC 3.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility End Stage Renal Disease NCT00157651

Eligibility End Stage Renal Disease NCT00157651

Inclusion Criteria
Description

Inclusion Criteria

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

newly placed double-lumen hemodialysis catheter

Data type

boolean

Alias
UMLS CUI [1]
C0019004
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
major bleed within last 3 months
Description

major bleeding

Data type

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)
Description

platelet count or coagulopathy

Data type

boolean

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

peptic ulcer disease

Data type

boolean

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

invasive intervention

Data type

boolean

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

warfarin

Data type

boolean

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

allergic to, or intolerant of, warfarin

Data type

boolean

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

pregnant

Data type

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
Description

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

Data type

boolean

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

catheter likely needed for 2 weeks or less

Data type

boolean

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

patient previously took part in the study

Data type

boolean

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

aortic aneurysm

Data type

boolean

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

patients nephrologist has refused consent

Data type

boolean

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

patient has refused consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430

Similar models

Eligibility End Stage Renal Disease NCT00157651

Name
Type
Description | Question | Decode (Coded Value)
Data type
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])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial