ID

13647

Description

Pharmacologic Reversal of Ventricular Remodeling in Childhood Cancer Survivors at Risk for Congestive Heart Failure (PREVENT-CHF): A Phase IIB Randomized Placebo-Controlled Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01347970

Link

https://clinicaltrials.gov/show/NCT01347970

Keywords

  1. 2/22/16 2/22/16 -
Uploaded on

February 22, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Cancer Survivor NCT01347970

Eligibility Cancer Survivor NCT01347970

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
cancer diagnosis prior to 22 years of age, irrespective of current age
Description

diagnosis cancer; age

Data type

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C0006826
UMLS CUI [2]
C0001779
lifetime cumulative anthracycline dose: >= 300 mg/m^2 without the protection of dexrazoxane (zinecard) therapy
Description

dose anthracycline; dexrazoxane

Data type

boolean

Alias
UMLS CUI [1,1]
C3174092
UMLS CUI [1,2]
C0282564
UMLS CUI [2]
C0086444
time from completion of cancer treatment to study entry: >= 2 years
Description

cancer treatment

Data type

boolean

Alias
UMLS CUI [1]
C0920425
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
receiving treatment for cardiomyopathy or congestive heart failure
Description

treatment cardiomyopathy; treatment congestive heart failure

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0878544
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0018802

Similar models

Eligibility Cancer Survivor NCT01347970

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
diagnosis cancer; age
Item
cancer diagnosis prior to 22 years of age, irrespective of current age
boolean
C0011900 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
dose anthracycline; dexrazoxane
Item
lifetime cumulative anthracycline dose: >= 300 mg/m^2 without the protection of dexrazoxane (zinecard) therapy
boolean
C3174092 (UMLS CUI [1,1])
C0282564 (UMLS CUI [1,2])
C0086444 (UMLS CUI [2])
cancer treatment
Item
time from completion of cancer treatment to study entry: >= 2 years
boolean
C0920425 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
treatment cardiomyopathy; treatment congestive heart failure
Item
receiving treatment for cardiomyopathy or congestive heart failure
boolean
C0087111 (UMLS CUI [1,1])
C0878544 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0018802 (UMLS CUI [2,2])

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