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ID
17910
Descripción
Vitalis Study - Observational Study on the Quality of Life in Patients Under Treatment for B-Chronic Lymphocytic Leukemia (B-CLL); ODM derived from: https://clinicaltrials.gov/show/NCT00344825
Link
https://clinicaltrials.gov/show/NCT00344825
Palabras clave
Versiones (2)
- 7/10/16 7/10/16 -
- 20/9/21 20/9/21 -
Subido en
7 de octubre de 2016
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility Leukemia, B-Cell, Chronic NCT00344825
Eligibility Leukemia, B-Cell, Chronic NCT00344825
- StudyEvent: Eligibility
Similar models
Eligibility Leukemia, B-Cell, Chronic NCT00344825
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Age
Item
aged >/=18 years
boolean
C0001779 (UMLS CUI [1])
Gender | Chronic Lymphocytic Leukemia | Pharmacotherapy New Chronic Lymphocytic Leukemia
Item
patients of either sex with b-cll, who are starting a new pharmacological treatment for b-chronic lymphocytic leukemia (1st, 2nd, 3rd, 4th)
boolean
C0079399 (UMLS CUI [1])
C0023434 (UMLS CUI [2])
C0013216 (UMLS CUI [3,1])
C0205314 (UMLS CUI [3,2])
C0023434 (UMLS CUI [3,3])
C0023434 (UMLS CUI [2])
C0013216 (UMLS CUI [3,1])
C0205314 (UMLS CUI [3,2])
C0023434 (UMLS CUI [3,3])
Duration of therapy Chronic Lymphocytic Leukemia
Item
foreseen duration of cll therapy </= 6 months
boolean
C0444917 (UMLS CUI [1,1])
C0023434 (UMLS CUI [1,2])
C0023434 (UMLS CUI [1,2])
Chronic Lymphocytic Leukemia | Binet Staging System | Rai Staging System
Item
b-chronic lymphocytic leukemia progressive stage a, stage b or c (according to binet system), or ii-iv (according to rai system)
boolean
C0023434 (UMLS CUI [1])
C1511118 (UMLS CUI [2])
C1514715 (UMLS CUI [3])
C1511118 (UMLS CUI [2])
C1514715 (UMLS CUI [3])
WHO performance status scale
Item
who performance status </= 2
boolean
C1298650 (UMLS CUI [1])
Life Expectancy
Item
life expectancy </= 6 months
boolean
C0023671 (UMLS CUI [1])
Informed Consent | Quality of life scale
Item
signed informed consent for personal data's treatment and availability to fill in the qol questionnaire
boolean
C0021430 (UMLS CUI [1])
C0451401 (UMLS CUI [2])
C0451401 (UMLS CUI [2])
Malignant Neoplasms
Item
patients with any other tumour disease
boolean
C0006826 (UMLS CUI [1])
Therapeutic procedure Chronic Lymphocytic Leukemia
Item
chronic lymphocytic leukemia therapy in the last 30 days before v0
boolean
C0087111 (UMLS CUI [1,1])
C0023434 (UMLS CUI [1,2])
C0023434 (UMLS CUI [1,2])
Therapeutic procedure Quantity Chronic Lymphocytic Leukemia
Item
more than 3 previous cll treatments (the therapy is defined by the drug and/or the treatment period)
boolean
C0087111 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0023434 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,2])
C0023434 (UMLS CUI [1,3])
Stem cell transplant
Item
previous stem cells transplantation
boolean
C1504389 (UMLS CUI [1])
Study Subject Participation Status
Item
concurrent or in the last 30 days participation to any other clinical trial
boolean
C2348568 (UMLS CUI [1])
medical condition Informed Consent Limited | medical condition Affecting Completion Quality of life scale | Mental condition Informed Consent Limited | Mental condition Affecting Completion Quality of life scale
Item
any medical or psychological conditions that might compromise the capacity to sign the consent for personal data's treatment or to fill in the qol questionnaire
boolean
C3843040 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0205197 (UMLS CUI [2,3])
C0451401 (UMLS CUI [2,4])
C3840291 (UMLS CUI [3,1])
C0021430 (UMLS CUI [3,2])
C0439801 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C0205197 (UMLS CUI [4,3])
C0451401 (UMLS CUI [4,4])
C0021430 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0205197 (UMLS CUI [2,3])
C0451401 (UMLS CUI [2,4])
C3840291 (UMLS CUI [3,1])
C0021430 (UMLS CUI [3,2])
C0439801 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C0205197 (UMLS CUI [4,3])
C0451401 (UMLS CUI [4,4])