Information:
Fel:
ID
20242
Beskrivning
The Effect of Ribose on B-Type Natriuretic Peptide (BNP) Levels in Congestive Heart Failure Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00329485
Länk
https://clinicaltrials.gov/show/NCT00329485
Nyckelord
Versioner (1)
- 2017-02-15 2017-02-15 -
Uppladdad den
15 februari 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Congestive Heart Failure NCT00329485
Eligibility Congestive Heart Failure NCT00329485
- StudyEvent: Eligibility
Similar models
Eligibility Congestive Heart Failure NCT00329485
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Adult Symptomatic | Age
Item
symptomatic adults, m/f, between 18 and 80 years of age
boolean
C0001675 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
C0231220 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Brain natriuretic peptide measurement
Item
bnp levels equal to or greater than 300 pg/ml.
boolean
C1095989 (UMLS CUI [1])
Congestive heart failure Principal diagnosis New York Heart Association Classification | Congestive heart failure Secondary diagnosis New York Heart Association Classification
Item
primary or secondary diagnosis of congestive heart failure at the time of admission (any nyha class)
boolean
C0018802 (UMLS CUI [1,1])
C0332137 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
C0018802 (UMLS CUI [2,1])
C0332138 (UMLS CUI [2,2])
C1275491 (UMLS CUI [2,3])
C0332137 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
C0018802 (UMLS CUI [2,1])
C0332138 (UMLS CUI [2,2])
C1275491 (UMLS CUI [2,3])
Congestive heart failure Disease length
Item
diagnosis of congestive heart failure for at least 3 months
boolean
C0018802 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0872146 (UMLS CUI [1,2])
6-minute walk test Perform Able
Item
able to perform 6 minute hall walk
boolean
C0430515 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C0884358 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Pharmacotherapy Class unchanged
Item
no therapeutic pharmaceutical class changes for at least 1 month
boolean
C0013216 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
C0442739 (UMLS CUI [1,3])
C0456387 (UMLS CUI [1,2])
C0442739 (UMLS CUI [1,3])
Informed Consent
Item
provide informed consent
boolean
C0021430 (UMLS CUI [1])
Study Subject Participation Status | Washout Period
Item
a 30-day washout period must be achieved for any patient involved in a previous clinical study.
boolean
C2348568 (UMLS CUI [1])
C1710661 (UMLS CUI [2])
C1710661 (UMLS CUI [2])
Exclusion Criteria
Item
exclusion
boolean
C0680251 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent
Item
insulin dependent diabetes (type i)
boolean
C0011854 (UMLS CUI [1])
Valvular disease Obstructive
Item
history of obstructive valvular disease
boolean
C3258293 (UMLS CUI [1,1])
C0549186 (UMLS CUI [1,2])
C0549186 (UMLS CUI [1,2])
Pulmonary Hypertension
Item
history of pulmonary hypertension within the last 3 months
boolean
C0020542 (UMLS CUI [1])
Hypertrophic Cardiomyopathy | Cardiomyopathy, Alcoholic
Item
history of hypertrophic or alcoholic cardiomyopathy
boolean
C0007194 (UMLS CUI [1])
C0007192 (UMLS CUI [2])
C0007192 (UMLS CUI [2])
Restrictive cardiomyopathy
Item
history of restrictive cardiomyopathy
boolean
C0007196 (UMLS CUI [1])
Cardiomyopathy Reversible
Item
history of reversible cardiomyopathy
boolean
C0878544 (UMLS CUI [1,1])
C0205343 (UMLS CUI [1,2])
C0205343 (UMLS CUI [1,2])
Patient Non-Compliance
Item
history of non-compliance
boolean
C0376405 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Study Subject Participation Status
Item
current enrollment in any other clinical study
boolean
C2348568 (UMLS CUI [1])