ID
20835
Description
RED-HF™ Trial - Reduction of Events With Darbepoetin Alfa in Heart Failure Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00358215
Link
https://clinicaltrials.gov/show/NCT00358215
Keywords
Versions (1)
- 3/21/17 3/21/17 -
Uploaded on
March 21, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Heart Failure NCT00358215
Eligibility Heart Failure NCT00358215
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Transferrin saturation measurement
Data type
boolean
Alias
- UMLS CUI [1]
- C1277709
Description
Blood Pressure
Data type
boolean
Alias
- UMLS CUI [1]
- C0005823
Description
Heart failure Due to Heart valve disease | Heart valve disease Causing Correction Surgical
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0018801
- UMLS CUI [1,2]
- C0678226
- UMLS CUI [1,3]
- C0018824
- UMLS CUI [2,1]
- C0018824
- UMLS CUI [2,2]
- C0678227
- UMLS CUI [2,3]
- C1947976
- UMLS CUI [2,4]
- C0543467
Description
Transplant Recipient Organ Major | Renal Replacement Therapy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0376387
- UMLS CUI [1,2]
- C0178784
- UMLS CUI [1,3]
- C0205164
- UMLS CUI [2]
- C0206074
Description
Creatinine measurement, serum
Data type
boolean
Alias
- UMLS CUI [1]
- C0201976
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Eligibility Heart Failure NCT00358215
- StudyEvent: Eligibility
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C1275491 (UMLS CUI [1,3])
C0678226 (UMLS CUI [1,2])
C0018824 (UMLS CUI [1,3])
C0018824 (UMLS CUI [2,1])
C0678227 (UMLS CUI [2,2])
C1947976 (UMLS CUI [2,3])
C0543467 (UMLS CUI [2,4])
C0178784 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
C0206074 (UMLS CUI [2])