ID

24239

Descripción

Investigation of Heart Failure Status Over Time Using Respiratory Parameters; ODM derived from: https://clinicaltrials.gov/show/NCT00494117

Link

https://clinicaltrials.gov/show/NCT00494117

Palabras clave

Versiones (1)
  1. 27/7/17 27/7/17 -
Subido en

27 de julio de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Heart Failure, Congestive NCT00494117

Inglés

Eligibility Heart Failure, Congestive NCT00494117

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
moderate to severe heart failure (as determined by echocardiogram or by treating physician)
Descripción

Heart failure Moderate Echocardiogram | Heart failure Severe Echocardiogram

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0205081
UMLS CUI [1,3]
C2243117
UMLS CUI [2,1]
C0018801
UMLS CUI [2,2]
C0205082
UMLS CUI [2,3]
C2243117
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
malignant disease affecting gas exchange or respiratory parameters
Descripción

Malignant disease Affecting Gas Exchange | Malignant disease Affecting Parameters respiratory

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0442867
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0017110
UMLS CUI [1,4]
C4019011
UMLS CUI [2,1]
C0442867
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C0449381
UMLS CUI [2,4]
C0521346
medications compromising breathing with no adverse affects on heart failure
Descripción

Pharmaceutical Preparations compromise Breathing | Adverse effects Heart failure Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C2945640
UMLS CUI [1,3]
C0035203
UMLS CUI [2,1]
C0879626
UMLS CUI [2,2]
C0018801
UMLS CUI [2,3]
C0332197
clinically significant (moderate to severe) asthma requiring therapy
Descripción

Moderate asthma Treatment required for | Severe asthma Treatment required for

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0581125
UMLS CUI [1,2]
C0332121
UMLS CUI [2,1]
C0581126
UMLS CUI [2,2]
C0332121
chronic parenchymal lung disease (fev1/fvc ratio = 65% or as determined by the treating physician)
Descripción

Chronic lung disease Parenchymal | FEV1/FVC ratio

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0746102
UMLS CUI [1,2]
C4277702
UMLS CUI [2]
C0429745
severe pulmonary hypertension
Descripción

Pulmonary Hypertension Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020542
UMLS CUI [1,2]
C0205082
heart failure due to alcohol abuse or chemotherapy
Descripción

Heart failure Due to Alcohol abuse | Heart failure Due to Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0085762
UMLS CUI [2,1]
C0018801
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0392920
narcotic abuse/intravenous drug use (including hiv+ and hepatitis c)
Descripción

Narcotic Abuse | intravenous drug use | HIV Seropositivity | Hepatitis C

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0524661
UMLS CUI [2]
C0699778
UMLS CUI [3]
C0019699
UMLS CUI [4]
C0019196
alcohol consumption > 80g/day
Descripción

Alcohol consumption U/day

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0001948
UMLS CUI [1,2]
C0456683
patients receiving home oxygen
Descripción

Home oxygen

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0421203
methicillin- resistant staphylococcus aureus infection
Descripción

Staphylococcus aureus infection | Methicillin Resistance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1318973
UMLS CUI [2]
C0079830
narcolepsy
Descripción

Narcolepsy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027404
cataplexy
Descripción

Cataplexy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007384
enrolled in any concurrent study, that may confound the results of this study.
Descripción

Study Subject Participation Status Interferes with Research results

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0683954
inability or refusal to sign the patient consent form
Descripción

Informed Consent Unable | Informed Consent Refused

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1705116
inability or refusal to adhere to protocol requirements
Descripción

Protocol Compliance Unable | Protocol Compliance Refused

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0525058
UMLS CUI [2,2]
C1705116
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Similar models

Eligibility Heart Failure, Congestive NCT00494117

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Heart failure Moderate Echocardiogram | Heart failure Severe Echocardiogram
Item
moderate to severe heart failure (as determined by echocardiogram or by treating physician)
boolean
C0018801 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C2243117 (UMLS CUI [1,3])
C0018801 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C2243117 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Malignant disease Affecting Gas Exchange | Malignant disease Affecting Parameters respiratory
Item
malignant disease affecting gas exchange or respiratory parameters
boolean
C0442867 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0017110 (UMLS CUI [1,3])
C4019011 (UMLS CUI [1,4])
C0442867 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0449381 (UMLS CUI [2,3])
C0521346 (UMLS CUI [2,4])
Pharmaceutical Preparations compromise Breathing | Adverse effects Heart failure Absent
Item
medications compromising breathing with no adverse affects on heart failure
boolean
C0013227 (UMLS CUI [1,1])
C2945640 (UMLS CUI [1,2])
C0035203 (UMLS CUI [1,3])
C0879626 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Moderate asthma Treatment required for | Severe asthma Treatment required for
Item
clinically significant (moderate to severe) asthma requiring therapy
boolean
C0581125 (UMLS CUI [1,1])
C0332121 (UMLS CUI [1,2])
C0581126 (UMLS CUI [2,1])
C0332121 (UMLS CUI [2,2])
Chronic lung disease Parenchymal | FEV1/FVC ratio
Item
chronic parenchymal lung disease (fev1/fvc ratio = 65% or as determined by the treating physician)
boolean
C0746102 (UMLS CUI [1,1])
C4277702 (UMLS CUI [1,2])
C0429745 (UMLS CUI [2])
Pulmonary Hypertension Severe
Item
severe pulmonary hypertension
boolean
C0020542 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Heart failure Due to Alcohol abuse | Heart failure Due to Chemotherapy
Item
heart failure due to alcohol abuse or chemotherapy
boolean
C0018801 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0085762 (UMLS CUI [1,3])
C0018801 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0392920 (UMLS CUI [2,3])
Narcotic Abuse | intravenous drug use | HIV Seropositivity | Hepatitis C
Item
narcotic abuse/intravenous drug use (including hiv+ and hepatitis c)
boolean
C0524661 (UMLS CUI [1])
C0699778 (UMLS CUI [2])
C0019699 (UMLS CUI [3])
C0019196 (UMLS CUI [4])
Alcohol consumption U/day
Item
alcohol consumption > 80g/day
boolean
C0001948 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
Home oxygen
Item
patients receiving home oxygen
boolean
C0421203 (UMLS CUI [1])
Staphylococcus aureus infection | Methicillin Resistance
Item
methicillin- resistant staphylococcus aureus infection
boolean
C1318973 (UMLS CUI [1])
C0079830 (UMLS CUI [2])
Narcolepsy
Item
narcolepsy
boolean
C0027404 (UMLS CUI [1])
Cataplexy
Item
cataplexy
boolean
C0007384 (UMLS CUI [1])
Study Subject Participation Status Interferes with Research results
Item
enrolled in any concurrent study, that may confound the results of this study.
boolean
C2348568 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
Informed Consent Unable | Informed Consent Refused
Item
inability or refusal to sign the patient consent form
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Protocol Compliance Unable | Protocol Compliance Refused
Item
inability or refusal to adhere to protocol requirements
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
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