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ID
27951
Description
Test of the Nipro ELISIO H Dialyzer in Different Dialysis Treatment Procedures; ODM derived from: https://clinicaltrials.gov/show/NCT00735059
Link
https://clinicaltrials.gov/show/NCT00735059
Keywords
Versions (2)
- 12/6/17 12/6/17 -
- 12/6/17 12/6/17 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
December 6, 2017
DOI
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License
Creative Commons BY-NC 3.0
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Eligibility Chronic Kidney Disease NCT00735059
Eligibility Chronic Kidney Disease NCT00735059
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Kidney Disease NCT00735059
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Age
Item
age ≥18 years
boolean
C0001779 (UMLS CUI [1])
Chronic Kidney Disease Stage | Hemodialysis | Hemodiafiltration
Item
ckd stage 5 with hemodialysis or hemodiafiltration treatment for more than three months
boolean
C1561643 (UMLS CUI [1,1])
C2074731 (UMLS CUI [1,2])
C0019004 (UMLS CUI [2])
C0206075 (UMLS CUI [3])
C2074731 (UMLS CUI [1,2])
C0019004 (UMLS CUI [2])
C0206075 (UMLS CUI [3])
Hematocrit measurement
Item
hematocrit >30 %
boolean
C0018935 (UMLS CUI [1])
Anticoagulation Therapy | Erythropoietin
Item
routine anticoagulation and erythropoietin regimen
boolean
C0003281 (UMLS CUI [1])
C0014822 (UMLS CUI [2])
C0014822 (UMLS CUI [2])
Vascular access complication Absent | Arteriovenous fistula | Graft | Catheter Flow Bidirectional
Item
no vascular access related problems (a/v-fistula, graft or bi-flow catheter)
boolean
C0920165 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0003855 (UMLS CUI [2])
C0332835 (UMLS CUI [3])
C0085590 (UMLS CUI [4,1])
C0806140 (UMLS CUI [4,2])
C1706937 (UMLS CUI [4,3])
C0332197 (UMLS CUI [1,2])
C0003855 (UMLS CUI [2])
C0332835 (UMLS CUI [3])
C0085590 (UMLS CUI [4,1])
C0806140 (UMLS CUI [4,2])
C1706937 (UMLS CUI [4,3])
Communicable Disease Absent
Item
no ongoing infection
boolean
C0009450 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
signed informed consent form
boolean
C0021430 (UMLS CUI [1])
Inclusion criteria failed
Item
inclusion criteria not met
boolean
C1512693 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])
HIV Infection PCR positive | Hepatitis B PCR positive | Hepatitis C PCR positive | Pregnancy
Item
known hiv or active hepatitis b or c infection (positive pcr). pregnancy
boolean
C0019693 (UMLS CUI [1,1])
C3888499 (UMLS CUI [1,2])
C0019163 (UMLS CUI [2,1])
C3888499 (UMLS CUI [2,2])
C0019196 (UMLS CUI [3,1])
C3888499 (UMLS CUI [3,2])
C0032961 (UMLS CUI [4])
C3888499 (UMLS CUI [1,2])
C0019163 (UMLS CUI [2,1])
C3888499 (UMLS CUI [2,2])
C0019196 (UMLS CUI [3,1])
C3888499 (UMLS CUI [3,2])
C0032961 (UMLS CUI [4])
Medical condition Unstable | Instability cardiac | Instability vascular
Item
unstable clinical condition (e.g. cardiac or vascular instability)
boolean
C3843040 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C1444783 (UMLS CUI [2,1])
C0018787 (UMLS CUI [2,2])
C1444783 (UMLS CUI [3,1])
C0005847 (UMLS CUI [3,2])
C0443343 (UMLS CUI [1,2])
C1444783 (UMLS CUI [2,1])
C0018787 (UMLS CUI [2,2])
C1444783 (UMLS CUI [3,1])
C0005847 (UMLS CUI [3,2])
Life Expectancy
Item
life expectancy less than 12 months
boolean
C0023671 (UMLS CUI [1])
Blood coagulation Problem
Item
known coagulation problems
boolean
C0005778 (UMLS CUI [1,1])
C0033213 (UMLS CUI [1,2])
C0033213 (UMLS CUI [1,2])
Study Subject Participation Status Interferes with Planned Study
Item
patients participating in another study interfering with the planned study
boolean
C2348568 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2347525 (UMLS CUI [1,3])
C0521102 (UMLS CUI [1,2])
C2347525 (UMLS CUI [1,3])