ID

34297

Description

HeRO Graft Compared to Permanent Catheters for End Stage Renal Disease (ESRD) Patients Receiving Hemodialysis; ODM derived from: https://clinicaltrials.gov/show/NCT01343251

Lien

https://clinicaltrials.gov/show/NCT01343251

Mots-clés

  1. 16/01/2019 16/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

16 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility End Stage Renal Disease (ESRD) NCT01343251

Eligibility End Stage Renal Disease (ESRD) NCT01343251

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
esrd patients requiring hemodialysis
Description

ID.1

Type de données

boolean

age > 18 years old
Description

ID.2

Type de données

boolean

able to give informed consent
Description

ID.3

Type de données

boolean

able to participate in quality of life survey
Description

ID.4

Type de données

boolean

all patients who are not candidate for avf or avg
Description

ID.5

Type de données

boolean

life expectancy 2 years or greater
Description

ID.6

Type de données

boolean

willing and able to participate with follow-up examinations
Description

ID.7

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or breastfeeding females
Description

ID.8

Type de données

boolean

disorder that compromises the ability to give informed consent and/or comply with the study procedures
Description

ID.9

Type de données

boolean

any medical condition that in the opinion of the investigator may pose a safety risk to a subject in the study or which may interfere with the study participation
Description

ID.10

Type de données

boolean

Similar models

Eligibility End Stage Renal Disease (ESRD) NCT01343251

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
esrd patients requiring hemodialysis
boolean
ID.2
Item
age > 18 years old
boolean
ID.3
Item
able to give informed consent
boolean
ID.4
Item
able to participate in quality of life survey
boolean
ID.5
Item
all patients who are not candidate for avf or avg
boolean
ID.6
Item
life expectancy 2 years or greater
boolean
ID.7
Item
willing and able to participate with follow-up examinations
boolean
Item Group
C0680251 (UMLS CUI)
ID.8
Item
pregnant or breastfeeding females
boolean
ID.9
Item
disorder that compromises the ability to give informed consent and/or comply with the study procedures
boolean
ID.10
Item
any medical condition that in the opinion of the investigator may pose a safety risk to a subject in the study or which may interfere with the study participation
boolean

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