ID
24237
Description
Evaluation of a Portable Device for Assessing Sleep Disordered Breathing in Congestive Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00493948
Link
https://clinicaltrials.gov/show/NCT00493948
Keywords
Versions (2)
- 7/27/17 7/27/17 -
- 7/27/17 7/27/17 -
Uploaded on
July 27, 2017
DOI
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License
Creative Commons BY-NC 3.0
Model comments :
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Eligibility Heart Failure, Congestive NCT00493948
Eligibility Heart Failure, Congestive NCT00493948
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Asthma Treatment required for
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0004096
- UMLS CUI [1,2]
- C0332121
Description
Lung disease Parenchymal
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0024115
- UMLS CUI [1,2]
- C4277702
Description
Pulmonary Hypertension Severe
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020542
- UMLS CUI [1,2]
- C0205082
Description
Hypercapnia | PCO2
Data type
boolean
Alias
- UMLS CUI [1]
- C0020440
- UMLS CUI [2]
- C0201931
Description
Shock, Cardiogenic
Data type
boolean
Alias
- UMLS CUI [1]
- C0036980
Description
Chronic Kidney Failure Severe
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0022661
- UMLS CUI [1,2]
- C0205082
Description
Narcotic Abuse | intravenous drug use | Heart failure Due to Alcohol abuse | Heart failure Due to Chemotherapy | Heart failure Due to HIV Seropositivity | Heart failure Due to Hepatitis C
Data type
boolean
Alias
- UMLS CUI [1]
- C0524661
- UMLS CUI [2]
- C0699778
- UMLS CUI [3,1]
- C0018801
- UMLS CUI [3,2]
- C0678226
- UMLS CUI [3,3]
- C0085762
- UMLS CUI [4,1]
- C0018801
- UMLS CUI [4,2]
- C0678226
- UMLS CUI [4,3]
- C0392920
- UMLS CUI [5,1]
- C0018801
- UMLS CUI [5,2]
- C0678226
- UMLS CUI [5,3]
- C0019699
- UMLS CUI [6,1]
- C0018801
- UMLS CUI [6,2]
- C0678226
- UMLS CUI [6,3]
- C0019196
Description
Staphylococcus aureus infection | Methicillin Resistance
Data type
boolean
Alias
- UMLS CUI [1]
- C1318973
- UMLS CUI [2]
- C0079830
Description
Tracheotomy
Data type
boolean
Alias
- UMLS CUI [1]
- C0040591
Description
Study Subject Participation Status Interferes with Research results
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2348568
- UMLS CUI [1,2]
- C0521102
- UMLS CUI [1,3]
- C0683954
Description
Airway pressure Positive Nocturnal | Oxygen Nocturnal
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0428719
- UMLS CUI [1,2]
- C1514241
- UMLS CUI [1,3]
- C0240526
- UMLS CUI [2,1]
- C0030054
- UMLS CUI [2,2]
- C0240526
Description
Informed Consent Unable | Informed Consent Refused
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C1299582
- UMLS CUI [2,1]
- C0021430
- UMLS CUI [2,2]
- C1705116
Description
Protocol Compliance Unable | Protocol Compliance Refused
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0525058
- UMLS CUI [1,2]
- C1299582
- UMLS CUI [2,1]
- C0525058
- UMLS CUI [2,2]
- C1705116
Similar models
Eligibility Heart Failure, Congestive NCT00493948
- StudyEvent: Eligibility
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])
C0332121 (UMLS CUI [1,2])
C4277702 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
C0201931 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C0699778 (UMLS CUI [2])
C0018801 (UMLS CUI [3,1])
C0678226 (UMLS CUI [3,2])
C0085762 (UMLS CUI [3,3])
C0018801 (UMLS CUI [4,1])
C0678226 (UMLS CUI [4,2])
C0392920 (UMLS CUI [4,3])
C0018801 (UMLS CUI [5,1])
C0678226 (UMLS CUI [5,2])
C0019699 (UMLS CUI [5,3])
C0018801 (UMLS CUI [6,1])
C0678226 (UMLS CUI [6,2])
C0019196 (UMLS CUI [6,3])
C0079830 (UMLS CUI [2])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C1514241 (UMLS CUI [1,2])
C0240526 (UMLS CUI [1,3])
C0030054 (UMLS CUI [2,1])
C0240526 (UMLS CUI [2,2])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])