Informations:
Erreur:
ID
23242
Description
Thalidomide Versus Bortezomib in Melphalan Refractory Myeloma; ODM derived from: https://clinicaltrials.gov/show/NCT00602511
Lien
https://clinicaltrials.gov/show/NCT00602511
Mots-clés
Versions (1)
- 30/06/2017 30/06/2017 -
Téléchargé le
30 juin 2017
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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 Multiple Myeloma NCT00602511
Eligibility Multiple Myeloma NCT00602511
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Myeloma NCT00602511
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
ID.1
Item
treatment demanding multiple myeloma
boolean
C0026764 (UMLS CUI [1])
ID.2
Item
refractoriness to melphalan
boolean
C0025241 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0205269 (UMLS CUI [1,2])
ID.3
Item
acceptance of rules for prevention of pregnancy
boolean
C0009862 (UMLS CUI [1])
ID.4
Item
previous treatment with bortezomib, thalidomide, or lenalidomide
boolean
C1176309 (UMLS CUI [1,1])
C0039736 (UMLS CUI [1,2])
C1144149 (UMLS CUI [1,3])
C0039736 (UMLS CUI [1,2])
C1144149 (UMLS CUI [1,3])
ID.5
Item
sensory neuropathy grade iii or neuropathic pain grade ii
boolean
C0151313 (UMLS CUI [1,1])
C0003892 (UMLS CUI [1,2])
C0003892 (UMLS CUI [1,2])
ID.6
Item
severe concomitant disorder, e.g. other malignancy or severe heart disease
boolean
C0012634 (UMLS CUI [1])
ID.7
Item
transformation to plasma cell leukemia or aggressive lymphoma
boolean
C0023484 (UMLS CUI [1,1])
C0024299 (UMLS CUI [1,2])
C0580822 (UMLS CUI [1,3])
C0024299 (UMLS CUI [1,2])
C0580822 (UMLS CUI [1,3])
ID.8
Item
frequent visits for bortezomib injections not feasible
boolean
C4276228 (UMLS CUI [1])
ID.9
Item
anticipated non-adherence to study protocol
boolean
C1321605 (UMLS CUI [1])
ID.10
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
ID.11
Item
anticipated non-adherence to rules for prevention of pregnancy
boolean
C1321605 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C0032961 (UMLS CUI [1,2])
ID.12
Item
severe thrombocytopenia (thrombocyte count less than 25000/microliter)
boolean
C0040034 (UMLS CUI [1])