Informations:
Erreur:
ID
13068
Description
SMD_FLAG-IDA_98: FLAG-IDA in Induction Treatment of High Risk Myelodysplastic Syndromes or Secondary Acute Myeloblastic Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT00487448
Lien
https://clinicaltrials.gov/show/NCT00487448
Mots-clés
Versions (1)
- 14/01/2016 14/01/2016 -
Détendeur de droits
CC BY-NC 3.0
Téléchargé le
14 janvier 2016
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 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 Myelodysplastic Syndrome NCT00487448
Eligibility Myelodysplastic Syndrome NCT00487448
- StudyEvent: Eligibility
Similar models
Eligibility Myelodysplastic Syndrome NCT00487448
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
age
Item
age < 75 years
boolean
C0001779 (UMLS CUI [1])
myelodysplastic syndrome
Item
diagnosis of myelodysplastic syndrome in order to fab criteria, excluding patients with chronic myeloid leukemia.
boolean
C3463824 (UMLS CUI [1])
IPI
Item
ipi > 1 (high risk or intermedia risk-2) and/or ipe equal or > 3 (high risk o intermedia risk) or secondary acute myeloid leukemia.
boolean
C1512894 (UMLS CUI [1])
toxicity
Item
resolved toxicity for previous treatments received to myelodysplastic syndrome .
boolean
C0600688 (UMLS CUI [1])
myelodysplastic syndrome de novo.
Item
myelodysplastic syndrome de novo.
boolean
C3463824 (UMLS CUI [1])
neoplasia
Item
associated neoplasia.
boolean
C1882062 (UMLS CUI [1])
chronic disease that can limit the patient follow up protocol
Item
chronic disease that can limit the patient follow up protocol (cardiovascular disease, active infection uncontrolled, etc.).
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
age < 55 years with related donor hla compatible
Item
age < 55 years with related donor hla compatible.
boolean
C0001779 (UMLS CUI [1])
C0019721 (UMLS CUI [2])
C0019721 (UMLS CUI [2])
investigational drug
Item
use an investigational drug in the 30 previous days.
boolean
C0013230 (UMLS CUI [1])
chemotherapy
Item
previous treatment with chemotherapy agents.
boolean
C0392920 (UMLS CUI [1])
simultaneous treatment
Item
simultaneous treatment during the study with other drugs not allowed in the protocol.
boolean
C0087111 (UMLS CUI [1])
bilirubin and gpt
Item
bilirubin > 2 mg/dl and gpt >2 times the normal value.
boolean
C1278039 (UMLS CUI [1])
C1557189 (UMLS CUI [2])
C1557189 (UMLS CUI [2])
creatinine
Item
creatinine > 2 mg/dl.
boolean
C0201976 (UMLS CUI [1])
hypersensibility
Item
hypersensibility to agents used in the protocol.
boolean
C0020517 (UMLS CUI [1])
secondary mds to chemo-radiotherapy .
Item
secondary mds to chemo-radiotherapy .
boolean
C3463824 (UMLS CUI [1])
hiv
Item
hiv positive.
boolean
C0019682 (UMLS CUI [1])
CML
Item
chronic myeloblastic leukemia
boolean
C0023474 (UMLS CUI [1])