Informações:
Falhas:
ID
12988
Descrição
A Pilot Study of OSI-461 in Patients With Chronic Lymphocytic Leukemia (CLL); ODM derived from: https://clinicaltrials.gov/show/NCT00073489
Link
https://clinicaltrials.gov/show/NCT00073489
Palavras-chave
Versões (1)
- 10/01/2016 10/01/2016 -
Transferido a
10 de janeiro de 2016
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Chronic Lymphocytic Leukemia NCT00073489
Eligibility Chronic Lymphocytic Leukemia NCT00073489
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Lymphocytic Leukemia NCT00073489
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
cll in biopsy or flow cytometry
Item
diagnosis of cll established by bone marrow aspiration and biopsy or flow cytometry of peripheral blood.
boolean
C0005558 (UMLS CUI [1,1])
C0023434 (UMLS CUI [1,2])
C0016263 (UMLS CUI [2,1])
C0023434 (UMLS CUI [2,2])
C0023434 (UMLS CUI [1,2])
C0016263 (UMLS CUI [2,1])
C0023434 (UMLS CUI [2,2])
therapy
Item
no previous therapy for cll.
boolean
C0087111 (UMLS CUI [1])
life expectancy
Item
expected remaining life span greater than or equal to six months.
boolean
C0023671 (UMLS CUI [1])
age
Item
18 years or older.
boolean
C0001779 (UMLS CUI [1])
informed consent
Item
willingness and ability to sign an informed consent.
boolean
C0021430 (UMLS CUI [1])
malignancy
Item
other active malignancy or history of treatment of any malignancy (excluding non-melanoma skin cancer) within the previous three years.
boolean
C0006826 (UMLS CUI [1])
malignancy
Item
history of other malignancy which could affect the diagnosis or assessment of osi-461.
boolean
C0006826 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
C0392760 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
therapy
Item
previous therapy for cll.
boolean
C0087111 (UMLS CUI [1])
Study Subject Participation Status
Item
use of an investigational medication or device within one month of initiating study therapy.
boolean
C2348568 (UMLS CUI [1])
immunotherapy
Item
concurrent immunotherapy.
boolean
C0021083 (UMLS CUI [1])
steroids
Item
use of steroids at the time of enrollment (patients who require steroids after enrollment may remain on study).
boolean
C0038317 (UMLS CUI [1])
comorbidity, medication
Item
any condition or any medication which may interfere with the conduct of the study.
boolean
C0009488 (UMLS CUI [1])
C0013227 (UMLS CUI [2])
C0013227 (UMLS CUI [2])
comorbidity
Item
serious uncontrolled intercurrent medical or psychiatric illness, including serious infection.
boolean
C0009488 (UMLS CUI [1])
cns involvement
Item
evidence of cns involvement.
boolean
C0449389 (UMLS CUI [1])
pregnancy, breastfeeding
Item
pregnant or nursing women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])