ID
44317
Beschrijving
Eligibility form Prüfung der Eignung zur Studienteilnahme NCT02905539 A Randomized, Double-blind Comparative Study Comparing Ferric Carboxymaltose (Ferinject) and Iron Isomaltoside 1000 (Monofer) for Iron Substitution in Iron-deficiency Anemia Quelle: Prof. Dr. med. Gunnar Heine Universitätsklinikum des Saarlandes
Trefwoorden
Versies (3)
- 09-07-17 09-07-17 -
- 28-12-17 28-12-17 -
- 20-09-21 20-09-21 -
Houder van rechten
Saarland University
Geüploaded op
20 september 2021
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility HOMe aFers 1 NCT02905539
Eligibility HOMe aFers 1 NCT02905539
- StudyEvent: ODM
Beschrijving
Prüfung der Ausschlusskriterien
Alias
- UMLS CUI-1
- C0680251
Beschrijving
Healthy Volunteers
Datatype
boolean
Alias
- UMLS CUI [1]
- C1708335
Beschrijving
Hypersensitivity to MonoFer or FERINJECT
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C2985193
- UMLS CUI [2,1]
- C0020517
- UMLS CUI [2,2]
- C2984025
Beschrijving
Severe hypersensitivity to other intravenous iron preparations
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C4305398
Beschrijving
Plasma phosphate < 2.5 mg/dL
Datatype
boolean
Alias
- UMLS CUI [1]
- C0523826
Beschrijving
Haemochromatosis
Datatype
boolean
Alias
- UMLS CUI [1]
- C0018995
Beschrijving
Untreated hyperparathyroidism
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0020502
- UMLS CUI [1,2]
- C0332155
Beschrijving
Renal replacement therapy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0206074
- UMLS CUI [2]
- C0022671
Beschrijving
Active malignant disease
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0205177
- UMLS CUI [1,2]
- C0006826
Beschrijving
Intravenous iron administration within the last 30 days
Datatype
boolean
Alias
- UMLS CUI [1]
- C4305398
Beschrijving
Treatment with erythropoietin or erythropoisis stimulating agents, red blood cell transfusion, radiotherapy, chemotherapy within the last 60 days
Datatype
boolean
Alias
- UMLS CUI [1]
- C0014822
- UMLS CUI [2]
- C1959590
- UMLS CUI [3]
- C0086252
- UMLS CUI [4]
- C1384668
- UMLS CUI [5]
- C3665472
Beschrijving
Surgery under anesthetic within the last 10 days
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0543467
- UMLS CUI [1,2]
- C0002932
Beschrijving
ASAT or ALAT 1.5-fold increased
Datatype
boolean
Alias
- UMLS CUI [1]
- C0201899
- UMLS CUI [2]
- C0201836
Beschrijving
Acute febrile infections within the last 7 days
Datatype
boolean
Alias
- UMLS CUI [1]
- C0948233
Beschrijving
Chronic inflammatory disease
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C3646020
- UMLS CUI [1,2]
- C1096024
Beschrijving
Self-reported severe asthma or eczema
Datatype
boolean
Alias
- UMLS CUI [1]
- C0581126
- UMLS CUI [2]
- C0013595
Beschrijving
Further contraindication (allergies, immunologic or inflammatory diseases)
Datatype
boolean
Alias
- UMLS CUI [1]
- C0522473
- UMLS CUI [2]
- C1527304
- UMLS CUI [3]
- C0021053
- UMLS CUI [4]
- C1290884
Beschrijving
Pregnancy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0032961
Beschrijving
Woman of childbearing potential without effective contraception method
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C4324275
- UMLS CUI [1,2]
- C0549184
- UMLS CUI [1,3]
- C0700589
Beschrijving
Lactating women
Datatype
boolean
Alias
- UMLS CUI [1]
- C0006147
Beschrijving
Present alcohol or drug dependency
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038580
Beschrijving
History of a psychological illness or seizures
Datatype
boolean
Alias
- UMLS CUI [1]
- C0004936
- UMLS CUI [2,1]
- C0205191
- UMLS CUI [2,2]
- C1540600
Beschrijving
Non-compliance or other study participation within the last 30 days
Datatype
boolean
Alias
- UMLS CUI [1]
- C0457432
- UMLS CUI [2,1]
- C0679823
- UMLS CUI [2,2]
- C1516648
Beschrijving
Ergebnis der Prüfung der Eignung zur Studienteilnahme
Alias
- UMLS CUI-1
- C0013893
- UMLS CUI-2
- C1274040
Beschrijving
Sind die Gründer für das Verletzen der Teilnahmebedingungen temporärer Natur, so kann in frühestens 14 Tagen eine erneute Screeninguntersuchung stattfinden.
Datatype
boolean
Alias
- UMLS CUI [1]
- C3242266
Beschrijving
Die Patientin kann an der Studie teilnehmen und muss im nächsten Schritt randomisiert werden.
Datatype
boolean
Alias
- UMLS CUI [1]
- C1302261
Beschrijving
Administrative Daten
Alias
- UMLS CUI-1
- C1320722
Similar models
Eligibility HOMe aFers 1 NCT02905539
- StudyEvent: ODM
C3163616 (UMLS CUI [1,2])
C1277709 (UMLS CUI [2])
C1744706 (UMLS CUI [1,2])
C3537005 (UMLS CUI [2,1])
C0235828 (UMLS CUI [2,2])
C2985193 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C2984025 (UMLS CUI [2,2])
C4305398 (UMLS CUI [1,2])
C0332155 (UMLS CUI [1,2])
C0022671 (UMLS CUI [2])
C0006826 (UMLS CUI [1,2])
C1959590 (UMLS CUI [2])
C0086252 (UMLS CUI [3])
C1384668 (UMLS CUI [4])
C3665472 (UMLS CUI [5])
C0002932 (UMLS CUI [1,2])
C0201836 (UMLS CUI [2])
C1096024 (UMLS CUI [1,2])
C0013595 (UMLS CUI [2])
C1527304 (UMLS CUI [2])
C0021053 (UMLS CUI [3])
C1290884 (UMLS CUI [4])
C0549184 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,3])
C0205191 (UMLS CUI [2,1])
C1540600 (UMLS CUI [2,2])
C0679823 (UMLS CUI [2,1])
C1516648 (UMLS CUI [2,2])
C1274040 (UMLS CUI-2)