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ID
17366
Beschrijving
Long Study - Longitudinal Thrombosis in End Stage Renal Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00157664
Link
https://clinicaltrials.gov/show/NCT00157664
Trefwoorden
Versies (1)
- 09-09-16 09-09-16 -
Geüploaded op
9 september 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility End Stage Renal Disease NCT00157664
Eligibility End Stage Renal Disease NCT00157664
- StudyEvent: Eligibility
Similar models
Eligibility End Stage Renal Disease NCT00157664
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Adult | Age
Item
adult patient (aged > 18 years)
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
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])
C0449238 (UMLS CUI [1,2])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
C0449238 (UMLS CUI [1,2])