Informatie:
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ID
29843
Beschrijving
Therapeutic Intensification of HIV-associated Non-Hodgkin's Lymphoma by Peripheral Blood Cell Transplantation Following Chemotherapy.; ODM derived from: https://clinicaltrials.gov/show/NCT00432419
Link
https://clinicaltrials.gov/show/NCT00432419
Trefwoorden
Versies (1)
- 23-04-18 23-04-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
23 april 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility HIV Infections NCT00432419
Eligibility HIV Infections NCT00432419
- StudyEvent: Eligibility
Similar models
Eligibility HIV Infections NCT00432419
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Adult | Age
Item
adult patients between 18 and 55 years old at screening
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
HIV-1 infection
Item
documented hiv-1 infection
boolean
C2363741 (UMLS CUI [1])
Antiretroviral Therapy, Highly Active
Item
currently haart-treated
boolean
C0887947 (UMLS CUI [1])
HIV Viral Load result
Item
plasma hiv-rna below 50 copies/ml at screening
boolean
C0019682 (UMLS CUI [1,1])
C0376705 (UMLS CUI [1,2])
C0376705 (UMLS CUI [1,2])
CD4 Positive T Lymphocytes Count | Lymphoma, Non-Hodgkin
Item
lymphocyte t cd4+ count above or equal to 100/mm3 at the nhl diagnosis
boolean
C0039215 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
C0024305 (UMLS CUI [2])
C0750480 (UMLS CUI [1,2])
C0024305 (UMLS CUI [2])
Non-Hodgkin Lymphoma Large Cell | Remission First | Prognostic Factor Poor IPI | Remission second
Item
histologically proven large cell nhl in first remission with classical poor prognostic factors (ipi above or equal to 2) or in second remission whatever ipi.
boolean
C0024305 (UMLS CUI [1,1])
C1513997 (UMLS CUI [1,2])
C0544452 (UMLS CUI [2,1])
C0205435 (UMLS CUI [2,2])
C1514474 (UMLS CUI [3,1])
C0542537 (UMLS CUI [3,2])
C1512894 (UMLS CUI [3,3])
C0544452 (UMLS CUI [4,1])
C0205436 (UMLS CUI [4,2])
C1513997 (UMLS CUI [1,2])
C0544452 (UMLS CUI [2,1])
C0205435 (UMLS CUI [2,2])
C1514474 (UMLS CUI [3,1])
C0542537 (UMLS CUI [3,2])
C1512894 (UMLS CUI [3,3])
C0544452 (UMLS CUI [4,1])
C0205436 (UMLS CUI [4,2])
Eligibility Criteria biological Intensive care
Item
biological criteria of eligibility for intensive therapeutic
boolean
C1516637 (UMLS CUI [1,1])
C0205460 (UMLS CUI [1,2])
C0085559 (UMLS CUI [1,3])
C0205460 (UMLS CUI [1,2])
C0085559 (UMLS CUI [1,3])
Informed Consent
Item
signed written informed consent
boolean
C0021430 (UMLS CUI [1])
Social security recipient
Item
patient protected by the social security of one of the european community countries.
boolean
C0682299 (UMLS CUI [1])
Burkitt Lymphoma
Item
burkitt nhl
boolean
C0006413 (UMLS CUI [1])
Non-Hodgkin's lymphoma of central nervous system
Item
central nervous system nhl
boolean
C2213246 (UMLS CUI [1])
Autologous hematopoietic stem cell transplant
Item
patients already treated by asct
boolean
C2193200 (UMLS CUI [1])
Communicable Disease
Item
ongoing infectious disease
boolean
C0009450 (UMLS CUI [1])
Mental disorder
Item
psychiatric disease
boolean
C0004936 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction < 25%
boolean
C0428772 (UMLS CUI [1])
Creatinine clearance measurement
Item
creatinine clearance < 50 ml/min
boolean
C0373595 (UMLS CUI [1])
Liver Failure
Item
hepatic failure
boolean
C0085605 (UMLS CUI [1])
Uncontrolled hypertension
Item
uncontrolled high blood pressure
boolean
C1868885 (UMLS CUI [1])
Hepatitis C, Chronic | Hepatitis B, Chronic
Item
chronic hepatitis c or b
boolean
C0524910 (UMLS CUI [1])
C0524909 (UMLS CUI [2])
C0524909 (UMLS CUI [2])
Study Subject Participation Status
Item
participating in other trials.
boolean
C2348568 (UMLS CUI [1])