ID

27953

Beschrijving

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

Trefwoorden

Versies (2)
  1. 06-12-17 06-12-17 -
  2. 06-12-17 06-12-17 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

6 december 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Chronic Kidney Disease NCT00735059

Engels

Eligibility Chronic Kidney Disease NCT00735059

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
age ≥18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ckd stage 5 with hemodialysis or hemodiafiltration treatment for more than three months
Beschrijving

Chronic Kidney Disease Stage | Hemodialysis | Hemodiafiltration

Datatype

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C2074731
UMLS CUI [2]
C0019004
UMLS CUI [3]
C0206075
hematocrit >30 %
Beschrijving

Hematocrit measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0018935
routine anticoagulation and erythropoietin regimen
Beschrijving

Anticoagulation Therapy | Erythropoietin

Datatype

boolean

Alias
UMLS CUI [1]
C0003281
UMLS CUI [2]
C0014822
no vascular access related problems (a/v-fistula, graft or bi-flow catheter)
Beschrijving

Vascular access complication Absent | Arteriovenous fistula | Graft | Catheter Flow Bidirectional

Datatype

boolean

Alias
UMLS CUI [1,1]
C0920165
UMLS CUI [1,2]
C0332197
UMLS CUI [2]
C0003855
UMLS CUI [3]
C0332835
UMLS CUI [4,1]
C0085590
UMLS CUI [4,2]
C0806140
UMLS CUI [4,3]
C1706937
no ongoing infection
Beschrijving

Communicable Disease Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0332197
signed informed consent form
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
inclusion criteria not met
Beschrijving

Inclusion criteria failed

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0231175
known hiv or active hepatitis b or c infection (positive pcr). pregnancy
Beschrijving

HIV Infection PCR positive | Hepatitis B PCR positive | Hepatitis C PCR positive | Pregnancy

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019693
UMLS CUI [1,2]
C3888499
UMLS CUI [2,1]
C0019163
UMLS CUI [2,2]
C3888499
UMLS CUI [3,1]
C0019196
UMLS CUI [3,2]
C3888499
UMLS CUI [4]
C0032961
unstable clinical condition (e.g. cardiac or vascular instability)
Beschrijving

Medical condition Unstable | Instability cardiac | Instability vascular

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0443343
UMLS CUI [2,1]
C1444783
UMLS CUI [2,2]
C0018787
UMLS CUI [3,1]
C1444783
UMLS CUI [3,2]
C0005847
life expectancy less than 12 months
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
known coagulation problems
Beschrijving

Blood coagulation Problem

Datatype

boolean

Alias
UMLS CUI [1,1]
C0005778
UMLS CUI [1,2]
C0033213
patients participating in another study interfering with the planned study
Beschrijving

Study Subject Participation Status Interferes with Planned Study

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2347525
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Similar models

Eligibility Chronic Kidney Disease NCT00735059

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
Communicable Disease Absent
Item
no ongoing infection
boolean
C0009450 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Informed Consent
Item
signed informed consent form
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Inclusion criteria failed
Item
inclusion criteria not met
boolean
C1512693 (UMLS CUI [1,1])
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])
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])
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])
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])
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