ID

17366

Description

Long Study - Longitudinal Thrombosis in End Stage Renal Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00157664

Link

https://clinicaltrials.gov/show/NCT00157664

Keywords

  1. 9/9/16 9/9/16 -
Uploaded on

September 9, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility End Stage Renal Disease NCT00157664

Eligibility End Stage Renal Disease NCT00157664

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patient (aged > 18 years)
Description

Adult | Age

Data type

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
patient on hemodialysis between 30 and 90 days
Description

Hemodialysis Duration

Data type

boolean

Alias
UMLS CUI [1,1]
C0019004
UMLS CUI [1,2]
C0449238
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
anticipated recovery of renal function (on dialysis < 90 days)
Description

Renal function Recovery Anticipated | Dialysis Duration

Data type

boolean

Alias
UMLS CUI [1,1]
C0232804
UMLS CUI [1,2]
C2004454
UMLS CUI [1,3]
C3840775
UMLS CUI [2,1]
C0011946
UMLS CUI [2,2]
C0449238
critical illness at time of recruitment (patients who are critically ill [icu] when first screened, who survive to 80 days, will be rescreened and will be able to participate at that point if no longer critically ill)
Description

Critical Illness | intensive care unit | Survival time | Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C0010340
UMLS CUI [2]
C0021708
UMLS CUI [3]
C2919552
UMLS CUI [4]
C2348568
planned live-donor renal transplant within 6 months
Description

Live donor renal transplant Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C0401177
UMLS CUI [1,2]
C1301732
patient cannot consent due to language barrier
Description

Informed Consent Unable Due to Language Barrier

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [1,3]
C0678226
UMLS CUI [1,4]
C0237167
patient cannot consent due to cognitive difficulties
Description

Informed Consent Unable Due to Impaired cognition

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [1,3]
C0678226
UMLS CUI [1,4]
C0338656
patient cannot consent due to hearing impairment
Description

Informed Consent Unable Due to hearing impairment

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [1,3]
C0678226
UMLS CUI [1,4]
C1384666
patient cannot consent due to speech impairment
Description

Informed Consent Unable Due to Speech impairment

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [1,3]
C0678226
UMLS CUI [1,4]
C0233715
patient or decision maker declines consent
Description

Informed Consent Refused

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705116
patient is unable to give consent and no substitute decision maker is available
Description

Informed Consent Unable | Patient Representative Unavailable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0030701
UMLS CUI [2,2]
C0686905
patient on dialysis longer than 90 days
Description

Dialysis Duration

Data type

boolean

Alias
UMLS CUI [1,1]
C0011946
UMLS CUI [1,2]
C0449238

Similar models

Eligibility End Stage Renal Disease NCT00157664

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age
Item
adult patient (aged > 18 years)
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Hemodialysis Duration
Item
patient on hemodialysis between 30 and 90 days
boolean
C0019004 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Renal function Recovery Anticipated | Dialysis Duration
Item
anticipated recovery of renal function (on dialysis < 90 days)
boolean
C0232804 (UMLS CUI [1,1])
C2004454 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,3])
C0011946 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Critical Illness | intensive care unit | Survival time | Study Subject Participation Status
Item
critical illness at time of recruitment (patients who are critically ill [icu] when first screened, who survive to 80 days, will be rescreened and will be able to participate at that point if no longer critically ill)
boolean
C0010340 (UMLS CUI [1])
C0021708 (UMLS CUI [2])
C2919552 (UMLS CUI [3])
C2348568 (UMLS CUI [4])
Live donor renal transplant Planned
Item
planned live-donor renal transplant within 6 months
boolean
C0401177 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Informed Consent Unable Due to Language Barrier
Item
patient cannot consent due to language barrier
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0678226 (UMLS CUI [1,3])
C0237167 (UMLS CUI [1,4])
Informed Consent Unable Due to Impaired cognition
Item
patient cannot consent due to cognitive difficulties
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0678226 (UMLS CUI [1,3])
C0338656 (UMLS CUI [1,4])
Informed Consent Unable Due to hearing impairment
Item
patient cannot consent due to hearing impairment
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0678226 (UMLS CUI [1,3])
C1384666 (UMLS CUI [1,4])
Informed Consent Unable Due to Speech impairment
Item
patient cannot consent due to speech impairment
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0678226 (UMLS CUI [1,3])
C0233715 (UMLS CUI [1,4])
Informed Consent Refused
Item
patient or decision maker declines consent
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Informed Consent Unable | Patient Representative Unavailable
Item
patient is unable to give consent and no substitute decision maker is available
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0030701 (UMLS CUI [2,1])
C0686905 (UMLS CUI [2,2])
Dialysis Duration
Item
patient on dialysis longer than 90 days
boolean
C0011946 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])

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