ID
28771
Description
Study of Herbal Formula Corresponding to Syndrome in Treating Post Percutaneous Coronary Intervention (PCI) Patients With Coronary Heart Disease (CHD); ODM derived from: https://clinicaltrials.gov/show/NCT00817024
Link
https://clinicaltrials.gov/show/NCT00817024
Keywords
Versions (1)
- 2/3/18 2/3/18 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
February 3, 2018
DOI
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License
Creative Commons BY 4.0
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Eligibility Coronary Heart Disease NCT00817024
Eligibility Coronary Heart Disease NCT00817024
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Symptomatic congestive heart failure New York Heart Association Classification
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0742758
- UMLS CUI [1,2]
- C1275491
Description
Pregnancy | Breast Feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Dysfunction Serious Organ Important | Liver Dysfunction Serious | Dysfunction Serious Lung | Renal dysfunction Serious
Data type
boolean
Alias
- UMLS CUI [1,1]
- C3887504
- UMLS CUI [1,2]
- C0205404
- UMLS CUI [1,3]
- C0178784
- UMLS CUI [1,4]
- C3898777
- UMLS CUI [2,1]
- C0086565
- UMLS CUI [2,2]
- C0205404
- UMLS CUI [3,1]
- C3887504
- UMLS CUI [3,2]
- C0205404
- UMLS CUI [3,3]
- C0024109
- UMLS CUI [4,1]
- C3279454
- UMLS CUI [4,2]
- C0205404
Description
Chinese herbal medicine
Data type
boolean
Alias
- UMLS CUI [1]
- C1273412
Description
Study Subject Participation Status
Data type
boolean
Alias
- UMLS CUI [1]
- C2348568
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Eligibility Coronary Heart Disease NCT00817024
- StudyEvent: Eligibility
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C1272703 (UMLS CUI [1,2])
C2936173 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
C2986501 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0205404 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,3])
C3898777 (UMLS CUI [1,4])
C0086565 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C3887504 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C0024109 (UMLS CUI [3,3])
C3279454 (UMLS CUI [4,1])
C0205404 (UMLS CUI [4,2])