Informatie:
Fout:
ID
31070
Beschrijving
Pilot Trial of Intravenous Vitamin C in Refractory Non-Hodgkin Lymphoma (NHL); ODM derived from: https://clinicaltrials.gov/show/NCT00626444
Link
https://clinicaltrials.gov/show/NCT00626444
Trefwoorden
Versies (1)
- 17-07-18 17-07-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
17 juli 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Non-Hodgkin Lymphoma NCT00626444
Eligibility Non-Hodgkin Lymphoma NCT00626444
- StudyEvent: Eligibility
Similar models
Eligibility Non-Hodgkin Lymphoma NCT00626444
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
age greater than 18 years old
boolean
C0001779 (UMLS CUI [1])
Aggressive NHL | Aggressive NHL Very
Item
aggressive or very aggressive nhl
boolean
C1332225 (UMLS CUI [1])
C1332225 (UMLS CUI [2,1])
C0442824 (UMLS CUI [2,2])
C1332225 (UMLS CUI [2,1])
C0442824 (UMLS CUI [2,2])
Therapeutic procedure Quantity failed
Item
failed one or more therapies
boolean
C0087111 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Disease Progression Absent
Item
patients must not have progressed within 60 days of last therapy
boolean
C0242656 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Allogeneic hematopoietic stem cell transplant Absent
Item
not received allogeneic stem cell transplant
boolean
C4255274 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Standard therapy Options Lacking
Item
no reasonable standard therapeutic options available
boolean
C2936643 (UMLS CUI [1,1])
C1518601 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
C1518601 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Glucose-6-phosphate dehydrogenase normal
Item
glucose 6 phosphate dehydrogenase status normal
boolean
C1167968 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Serum creatinine normal | Transaminases Normal
Item
normal creatinine and transaminase
boolean
C0438244 (UMLS CUI [1])
C0002594 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])
C0002594 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])
Childbearing Potential Pregnancy test negative
Item
women of child-bearing potential confirm negative pregnancy test
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
C0427780 (UMLS CUI [1,2])
Comorbidity Significant
Item
significant co-morbid disorders
boolean
C0009488 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0750502 (UMLS CUI [1,2])
Psychiatric symptom Significant
Item
significant psychiatric symptoms
boolean
C0233401 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0750502 (UMLS CUI [1,2])
Tobacco use
Item
smoking
boolean
C0543414 (UMLS CUI [1])
Alcohol intake above recommended sensible limits | Drug use Excessive
Item
excessive alcohol or drug use
boolean
C0560219 (UMLS CUI [1])
C2239127 (UMLS CUI [2,1])
C0442802 (UMLS CUI [2,2])
C2239127 (UMLS CUI [2,1])
C0442802 (UMLS CUI [2,2])
Study Subject Participation Status | Therapy, Investigational
Item
enrollment in other experimental therapy
boolean
C2348568 (UMLS CUI [1])
C0949266 (UMLS CUI [2])
C0949266 (UMLS CUI [2])
Communicable Disease
Item
active infection
boolean
C0009450 (UMLS CUI [1])
Disease Response | Therapeutic procedure Recent
Item
patients experiencing ongoing response to recent treatments
boolean
C1704632 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
Chemotherapy | Biological treatment
Item
patients who have received chemotherapy within 30 days or biological therapy within 6 weeks
boolean
C0392920 (UMLS CUI [1])
C1531518 (UMLS CUI [2])
C1531518 (UMLS CUI [2])
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