ID

20242

Descripción

The Effect of Ribose on B-Type Natriuretic Peptide (BNP) Levels in Congestive Heart Failure Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00329485

Link

https://clinicaltrials.gov/show/NCT00329485

Palabras clave

Versiones (1)
  1. 15/2/17 15/2/17 -
Subido en

15 de febrero de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Congestive Heart Failure NCT00329485

Inglés

Eligibility Congestive Heart Failure NCT00329485

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
symptomatic adults, m/f, between 18 and 80 years of age
Descripción

Adult Symptomatic | Age

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0001675
UMLS CUI [1,2]
C0231220
UMLS CUI [2]
C0001779
bnp levels equal to or greater than 300 pg/ml.
Descripción

Brain natriuretic peptide measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1095989
primary or secondary diagnosis of congestive heart failure at the time of admission (any nyha class)
Descripción

Congestive heart failure Principal diagnosis New York Heart Association Classification | Congestive heart failure Secondary diagnosis New York Heart Association Classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0332137
UMLS CUI [1,3]
C1275491
UMLS CUI [2,1]
C0018802
UMLS CUI [2,2]
C0332138
UMLS CUI [2,3]
C1275491
diagnosis of congestive heart failure for at least 3 months
Descripción

Congestive heart failure Disease length

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0872146
able to perform 6 minute hall walk
Descripción

6-minute walk test Perform Able

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0430515
UMLS CUI [1,2]
C0884358
UMLS CUI [1,3]
C0085732
no therapeutic pharmaceutical class changes for at least 1 month
Descripción

Pharmacotherapy Class unchanged

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0456387
UMLS CUI [1,3]
C0442739
provide informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
a 30-day washout period must be achieved for any patient involved in a previous clinical study.
Descripción

Study Subject Participation Status | Washout Period

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C1710661
exclusion
Descripción

Exclusion Criteria

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0680251
insulin dependent diabetes (type i)
Descripción

Diabetes Mellitus, Insulin-Dependent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011854
history of obstructive valvular disease
Descripción

Valvular disease Obstructive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3258293
UMLS CUI [1,2]
C0549186
history of pulmonary hypertension within the last 3 months
Descripción

Pulmonary Hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0020542
history of hypertrophic or alcoholic cardiomyopathy
Descripción

Hypertrophic Cardiomyopathy | Cardiomyopathy, Alcoholic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007194
UMLS CUI [2]
C0007192
history of restrictive cardiomyopathy
Descripción

Restrictive cardiomyopathy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007196
history of reversible cardiomyopathy
Descripción

Cardiomyopathy Reversible

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0878544
UMLS CUI [1,2]
C0205343
history of non-compliance
Descripción

Patient Non-Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0376405
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
current enrollment in any other clinical study
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Congestive Heart Failure NCT00329485

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
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])
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])
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])
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])
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])
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])
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])
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