ID
23600
Description
Responsible Party: Saarland University ClinicalTrials.gov Identifier: NCT02905539 History of Changes Other Study ID Numbers: P-0101 2015-004808-36 ( EudraCT Number ) U1111-1176-4563 ( Registry Identifier: WHO Universal Trial Number ) DRKS00010766 ( Registry Identifier: Deutsches Register Klinischer Studien ) Study First Received: September 8, 2016 Last Updated: September 13, 2016 A Study Comparing the Iron Substitution With the Medicinal Products Ferinject or Monofer (HOMe_aFers_1) ODM derived from: https://clinicaltrials.gov/ct2/show/NCT02905539
Lien
https://clinicaltrials.gov/ct2/show/NCT02905539
Mots-clés
Versions (3)
- 09/07/2017 09/07/2017 -
- 28/12/2017 28/12/2017 -
- 20/09/2021 20/09/2021 -
Téléchargé le
9 juillet 2017
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC-ND 3.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility Anemia NCT02905539 DRKS00010766
Eligibility Anemia NCT02905539 DRKS00010766
- StudyEvent: ODM
Description
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Description
Control Group
Type de données
boolean
Alias
- UMLS CUI [1]
- C0009932
Description
Hypersensitivity to iron supplement
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0721124
Description
Hypersensitivity
Type de données
boolean
Alias
- UMLS CUI [1]
- C0020517
Description
Plasma Phosphate
Type de données
boolean
Alias
- UMLS CUI [1]
- C1276038
Description
Hemochromatosis
Type de données
boolean
Alias
- UMLS CUI [1]
- C0018995
Description
Hyperparathyroidism
Type de données
boolean
Alias
- UMLS CUI [1]
- C0020502
Description
Renal replacement therapy, Kidney transplantation
Type de données
boolean
Alias
- UMLS CUI [1]
- C0206074
- UMLS CUI [2]
- C0022671
Description
Malignancy
Type de données
boolean
Alias
- UMLS CUI [1]
- C0006826
Description
Intravenous iron administration
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0013125
- UMLS CUI [1,2]
- C0721124
Description
Treatment
Type de données
boolean
Alias
- UMLS CUI [1]
- C0087111
Description
Surgery
Type de données
boolean
Alias
- UMLS CUI [1]
- C0543467
Description
ALT, AST
Type de données
boolean
Alias
- UMLS CUI [1]
- C0201836
- UMLS CUI [2]
- C0201899
Description
Febrile infection
Type de données
boolean
Alias
- UMLS CUI [1]
- C0948233
Description
Chronic inflammatory diseases
Type de données
boolean
Alias
- UMLS CUI [1]
- C1290886
Description
Asthma or eczema
Type de données
boolean
Alias
- UMLS CUI [1]
- C0004096
- UMLS CUI [2]
- C0013595
Description
Contraindication
Type de données
boolean
Alias
- UMLS CUI [1]
- C1301624
Description
Pregnancy
Type de données
boolean
Alias
- UMLS CUI [1]
- C0032961
Description
Contraceptive Methods
Type de données
boolean
Alias
- UMLS CUI [1]
- C0700589
Description
Lactating
Type de données
boolean
Alias
- UMLS CUI [1]
- C2828358
Description
Substance Use Disorder
Type de données
boolean
Alias
- UMLS CUI [1]
- C0038586
Description
Mental disorder, Seizures
Type de données
boolean
Alias
- UMLS CUI [1]
- C0004936
- UMLS CUI [2]
- C0036572
Description
Compliance
Type de données
boolean
Alias
- UMLS CUI [1]
- C1321605
Similar models
Eligibility Anemia NCT02905539 DRKS00010766
- StudyEvent: ODM
C3163616 (UMLS CUI [1,2])
C1277709 (UMLS CUI [2])
C1744706 (UMLS CUI [1,2])
C0721124 (UMLS CUI [1,2])
C0022671 (UMLS CUI [2])
C0721124 (UMLS CUI [1,2])
C0201899 (UMLS CUI [2])
C0013595 (UMLS CUI [2])
C0036572 (UMLS CUI [2])