ID

21290

Description

Endothelin Receptor Antagonism in Proteinuric Nephropathy; ODM derived from: https://clinicaltrials.gov/show/NCT00722215

Lien

https://clinicaltrials.gov/show/NCT00722215

Mots-clés

  1. 17/04/2017 17/04/2017 -
Téléchargé le

17 avril 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Chronic Kidney Disease NCT00722215

Eligibility Chronic Kidney Disease NCT00722215

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female
Description

gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
age 18-70
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
body mass index <35
Description

bmi

Type de données

boolean

Alias
UMLS CUI [1]
C1305855
blood pressure <160/110 mmhg
Description

blood pressure

Type de données

boolean

Alias
UMLS CUI [1]
C0005823
ckd stage 2-5 as per the k/doqi classification
Description

chronic kidney disease stage k/doqi classification

Type de données

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C2074731
UMLS CUI [1,3]
C2074730
proteinuria in one of the following categories: 0.3-1.5, >1.5-3.0, and >3.0-6.0 g/24hrs
Description

proteinuria

Type de données

boolean

Alias
UMLS CUI [1]
C0033687
normal serum albumin
Description

serum albumin

Type de données

boolean

Alias
UMLS CUI [1]
C0036773
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject is below the age of legal consent, or is mentally or legally incapacitated
Description

informed consent ability

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0085732
history of multiple and/or severe allergic reactions to drugs (including study drugs), or food
Description

drug or food allergy

Type de données

boolean

Alias
UMLS CUI [1]
C0013182
UMLS CUI [2]
C0016470
the subject has donated blood (450 ml) within the last 4 weeks
Description

blood donation

Type de données

boolean

Alias
UMLS CUI [1]
C0005794
past or present drug or alcohol abuse including intravenous drug abuse at any time
Description

drug or alcohol abuse

Type de données

boolean

Alias
UMLS CUI [1]
C0038586
participation in another clinical trial within 1 month
Description

clinical trial participation

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
considered to be at high risk of hiv or hepatitis b
Description

hiv or hepatitis b risk

Type de données

boolean

Alias
UMLS CUI [1]
C0744979
UMLS CUI [2,1]
C0019163
UMLS CUI [2,2]
C0035647
pregnant
Description

pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961

Similar models

Eligibility Chronic Kidney Disease NCT00722215

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
age
Item
age 18-70
boolean
C0001779 (UMLS CUI [1])
bmi
Item
body mass index <35
boolean
C1305855 (UMLS CUI [1])
blood pressure
Item
blood pressure <160/110 mmhg
boolean
C0005823 (UMLS CUI [1])
chronic kidney disease stage k/doqi classification
Item
ckd stage 2-5 as per the k/doqi classification
boolean
C1561643 (UMLS CUI [1,1])
C2074731 (UMLS CUI [1,2])
C2074730 (UMLS CUI [1,3])
proteinuria
Item
proteinuria in one of the following categories: 0.3-1.5, >1.5-3.0, and >3.0-6.0 g/24hrs
boolean
C0033687 (UMLS CUI [1])
serum albumin
Item
normal serum albumin
boolean
C0036773 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
informed consent ability
Item
subject is below the age of legal consent, or is mentally or legally incapacitated
boolean
C0021430 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
drug or food allergy
Item
history of multiple and/or severe allergic reactions to drugs (including study drugs), or food
boolean
C0013182 (UMLS CUI [1])
C0016470 (UMLS CUI [2])
blood donation
Item
the subject has donated blood (450 ml) within the last 4 weeks
boolean
C0005794 (UMLS CUI [1])
drug or alcohol abuse
Item
past or present drug or alcohol abuse including intravenous drug abuse at any time
boolean
C0038586 (UMLS CUI [1])
clinical trial participation
Item
participation in another clinical trial within 1 month
boolean
C2348568 (UMLS CUI [1])
hiv or hepatitis b risk
Item
considered to be at high risk of hiv or hepatitis b
boolean
C0744979 (UMLS CUI [1])
C0019163 (UMLS CUI [2,1])
C0035647 (UMLS CUI [2,2])
pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])

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