ID
11850
Description
Epoetin Alfa Biosimilar in the Management of Chemotherapy-Induced Symptomatic Anemia in Haematology and Oncology; ODM derived from: https://clinicaltrials.gov/show/NCT02140736
Lien
https://clinicaltrials.gov/show/NCT02140736
Mots-clés
Versions (1)
- 10/08/2015 10/08/2015 - Julian Varghese
Téléchargé le
10 août 2015
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Chemotherapy-induced Symptomatic Anemia NCT02140736
Eligibility Chemotherapy-induced Symptomatic Anemia NCT02140736
- StudyEvent: test
Description
Exclusion Criteria
Description
patients are not receiving chemotherapy
Type de données
boolean
Alias
- UMLS CUI [1]
- C3665472
Description
patients already included in an epoetin zeta trial
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2242969
- UMLS CUI [1,2]
- C1997870
Description
patients presenting with a contraindication to epoetin zeta
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0522473
- UMLS CUI [1,2]
- C1997870
Description
patients presenting with hypersensitivity to the active principle or any of the excipients
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0014822
Description
patient with erythroblastopenia or acquired pure red cell aplasia (aprca)
Type de données
boolean
Alias
- UMLS CUI [1]
- C0877221
- UMLS CUI [2]
- C0340961
Description
patient with uncontrollable arterial hypertension
Type de données
boolean
Alias
- UMLS CUI [1]
- C1868885
Description
patients who cannot receive adequate prophylaxis by antithrombotic agents
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0522473
- UMLS CUI [1,2]
- C1704311
Similar models
Eligibility Chemotherapy-induced Symptomatic Anemia NCT02140736
- StudyEvent: test
C0002871 (UMLS CUI [2])
C3665472 (UMLS CUI [2])
C0376545 (UMLS CUI [3])
C0357126 (UMLS CUI [1,2])
C1997870 (UMLS CUI [1,2])
C1997870 (UMLS CUI [1,2])
C0014822 (UMLS CUI [1,2])
C0340961 (UMLS CUI [2])
C1704311 (UMLS CUI [1,2])
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