ID
44039
Description
Effect of Dialysis on the Pharmacokinetics of Telavancin in Patients With Chronic Kidney Disease Stage 5; ODM derived from: https://clinicaltrials.gov/show/NCT02392208
Link
https://clinicaltrials.gov/show/NCT02392208
Keywords
Versions (2)
- 3/28/19 3/28/19 -
- 9/20/21 9/20/21 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
September 20, 2021
DOI
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License
Creative Commons BY 4.0
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Eligibility End-Stage Renal Disease NCT02392208
Eligibility End-Stage Renal Disease NCT02392208
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Hemoglobin measurement
Data type
boolean
Alias
- UMLS CUI [1]
- C0518015
Description
Measurement of albumin in plasma
Data type
boolean
Alias
- UMLS CUI [1]
- C3525688
Description
Pregnancy
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
Description
Breast Feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0006147
Description
Prolonged QTc interval on ECG
Data type
boolean
Alias
- UMLS CUI [1]
- C4015677
Description
Pharmaceutical Preparations Causing Prolonged QT interval
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0678227
- UMLS CUI [1,3]
- C0151878
Description
Warfarin | Heparin, Low-Molecular-Weight
Data type
boolean
Alias
- UMLS CUI [1]
- C0043031
- UMLS CUI [2]
- C0019139
Description
Hypersensitivity Telavancin | Vancomycin allergy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C1453642
- UMLS CUI [2]
- C0571388
Description
Unstable blood pressure Control
Data type
boolean
Alias
- UMLS CUI [1,1]
- C4540782
- UMLS CUI [1,2]
- C2587213
Description
Patient need for Removal Fluid Large | Dialysis procedure
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0686904
- UMLS CUI [1,2]
- C1883720
- UMLS CUI [1,3]
- C0005889
- UMLS CUI [1,4]
- C0549177
- UMLS CUI [2]
- C0011946
Description
Liver disease Child-Pugh Classification
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0023895
- UMLS CUI [1,2]
- C4050412
Description
Dialysis | Need for isolation Due to Hepatitis B
Data type
boolean
Alias
- UMLS CUI [1]
- C0011946
- UMLS CUI [2,1]
- C0260397
- UMLS CUI [2,2]
- C0678226
- UMLS CUI [2,3]
- C0019163
Description
Study Subject Participation Status | Investigational New Drugs
Data type
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0013230
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Eligibility End-Stage Renal Disease NCT02392208
- StudyEvent: Eligibility
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C4040576 (UMLS CUI [2])
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C0332197 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0678227 (UMLS CUI [1,2])
C0151878 (UMLS CUI [1,3])
C0019139 (UMLS CUI [2])
C1453642 (UMLS CUI [1,2])
C0571388 (UMLS CUI [2])
C2587213 (UMLS CUI [1,2])
C1883720 (UMLS CUI [1,2])
C0005889 (UMLS CUI [1,3])
C0549177 (UMLS CUI [1,4])
C0011946 (UMLS CUI [2])
C4050412 (UMLS CUI [1,2])
C0260397 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0019163 (UMLS CUI [2,3])
C0013230 (UMLS CUI [2])