Informações:
Falhas:
ID
30885
Descrição
Quality of Life of Non-transplant Candidate Multiple Myeloma Patients Treated With Early Bortezomib; ODM derived from: https://clinicaltrials.gov/show/NCT01060202
Link
https://clinicaltrials.gov/show/NCT01060202
Palavras-chave
Versões (1)
- 02/07/2018 02/07/2018 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
2 de julho de 2018
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Multiple Myeloma NCT01060202
Eligibility Multiple Myeloma NCT01060202
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Myeloma NCT01060202
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Multiple Myeloma Symptomatic
Item
symptomatic multiple myeloma patient
boolean
C0026764 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0231220 (UMLS CUI [1,2])
ECOG performance status
Item
ecog score less than 3
boolean
C1520224 (UMLS CUI [1])
Patients Inappropriate Stem cell transplant
Item
patient is not a candidate for stem cell transplantation
boolean
C0030705 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C1504389 (UMLS CUI [1,3])
C1548788 (UMLS CUI [1,2])
C1504389 (UMLS CUI [1,3])
Prior Therapy Duration
Item
previous treatment duration is less than 6 months
boolean
C1514463 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Prior Therapy Partial response failed
Item
previous treatment response is less than partial response (pr)
boolean
C1514463 (UMLS CUI [1,1])
C1521726 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C1521726 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Questionnaire Completion Willing | Questionnaire Completion Able
Item
willing and able to complete the questionnaire
boolean
C0034394 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
C0034394 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0085732 (UMLS CUI [2,3])
C0205197 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
C0034394 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0085732 (UMLS CUI [2,3])
Informed Consent | Informed Consent Patient Representatives
Item
patients (or their legally acceptable representatives) must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
Hypersensitivity Bortezomib
Item
known hypersensitivity to bortezomib
boolean
C0020517 (UMLS CUI [1,1])
C1176309 (UMLS CUI [1,2])
C1176309 (UMLS CUI [1,2])
Communicable Disease Severe Requirement Antibiotic therapy
Item
acute severe infection requiring antibiotics therapy
boolean
C0009450 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C0338237 (UMLS CUI [1,4])
C0205082 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C0338237 (UMLS CUI [1,4])
Peripheral Neuropathy Pre-existing CTCAE Grades
Item
pre-existing peripheral neuropathy greater than or equal to grade 2
boolean
C0031117 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
C1516728 (UMLS CUI [1,3])
C2347662 (UMLS CUI [1,2])
C1516728 (UMLS CUI [1,3])
Cardiovascular Disease Uncontrolled | Cardiovascular Disease Severe
Item
uncontrolled or severe cardiovascular disease
boolean
C0007222 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0205318 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])