ID

15403

Beschrijving

Reversal of Ventricular Remodeling With Toprol-XL; ODM derived from: https://clinicaltrials.gov/show/NCT00038077

Link

https://clinicaltrials.gov/show/NCT00038077

Trefwoorden

  1. 30-05-16 30-05-16 -
Geüploaded op

30 mei 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Heart Failure, Congestive NCT00038077

Eligibility Heart Failure, Congestive NCT00038077

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of stable asymptomatic heart failure.
Beschrijving

heart failure, stable, asymptomatic

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0231221
documented ejection fraction less than 0.40.
Beschrijving

lvef

Datatype

boolean

Alias
UMLS CUI [1]
C0428772
must be able to comply with all study procedures.
Beschrijving

ability to comply

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
taken b-blocker therapy for longer than 1 week within 6 months prior to randomization.
Beschrijving

beta-blocker

Datatype

boolean

Alias
UMLS CUI [1]
C0001645
have heart problems that would not allow b-blocker therapy.
Beschrijving

heart problems contraindicating beta-blockers

Datatype

boolean

Alias
UMLS CUI [1,1]
C0795691
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C0001645
receiving b-blockers therapy for any medical reason including topical b-blockers that might cause systemic absorption (e.g., glaucoma).
Beschrijving

beta-blockers

Datatype

boolean

Alias
UMLS CUI [1]
C0304516
undergone certain heart surgeries, such as, prior heart transplant or cardiomyoplasty.
Beschrijving

heart surgery

Datatype

boolean

Alias
UMLS CUI [1]
C0018821
have certain heart diseases.
Beschrijving

heart diseases

Datatype

boolean

Alias
UMLS CUI [1]
C0018799
pregnant or breast feeding.
Beschrijving

pregnancy; breast feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
unlikely to survive.
Beschrijving

life expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671

Similar models

Eligibility Heart Failure, Congestive NCT00038077

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
heart failure, stable, asymptomatic
Item
diagnosis of stable asymptomatic heart failure.
boolean
C0018801 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0231221 (UMLS CUI [1,3])
lvef
Item
documented ejection fraction less than 0.40.
boolean
C0428772 (UMLS CUI [1])
ability to comply
Item
must be able to comply with all study procedures.
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
beta-blocker
Item
taken b-blocker therapy for longer than 1 week within 6 months prior to randomization.
boolean
C0001645 (UMLS CUI [1])
heart problems contraindicating beta-blockers
Item
have heart problems that would not allow b-blocker therapy.
boolean
C0795691 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0001645 (UMLS CUI [1,3])
beta-blockers
Item
receiving b-blockers therapy for any medical reason including topical b-blockers that might cause systemic absorption (e.g., glaucoma).
boolean
C0304516 (UMLS CUI [1])
heart surgery
Item
undergone certain heart surgeries, such as, prior heart transplant or cardiomyoplasty.
boolean
C0018821 (UMLS CUI [1])
heart diseases
Item
have certain heart diseases.
boolean
C0018799 (UMLS CUI [1])
pregnancy; breast feeding
Item
pregnant or breast feeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
life expectancy
Item
unlikely to survive.
boolean
C0023671 (UMLS CUI [1])

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