Informatie:
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ID
12918
Beschrijving
Vaccination of Follicular Lymphomas With Tumor-Derived Immunoglobulin Idiotype; ODM derived from: https://clinicaltrials.gov/show/NCT00001572
Link
https://clinicaltrials.gov/show/NCT00001572
Trefwoorden
Versies (1)
- 06-01-16 06-01-16 -
Houder van rechten
CC BY-NC 3.0
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6 januari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility B Cell Lymphoma NCT00001572
Eligibility B Cell Lymphoma NCT00001572
- StudyEvent: Eligibility
Similar models
Eligibility B Cell Lymphoma NCT00001572
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
sex
Item
sex distribution: male and female.
boolean
C0079399 (UMLS CUI [1])
age
Item
age: patients must be greater than or equal to 18 years old.
boolean
C0001779 (UMLS CUI [1])
eligibility criteria
Item
patients must meet all of the following eligibility criteria:
boolean
C1512693 (UMLS CUI [1])
lymphoma
Item
tissue diagnosis of: follicular small cleaved cell or follicular mixed lymphoma with surface igm, iga, or igg phenotype with a monoclonal heavy and light chain. pathology slides must be submitted to the nih pathology department for review.
boolean
C0024299 (UMLS CUI [1])
tumor stage
Item
stage iii or iv lymphoma.
boolean
C1300072 (UMLS CUI [1])
lymph node
Item
a single peripheral lymph node of at least 2x2 to 3x3 cm size and accessible for biopsy/harvest.
boolean
C0024204 (UMLS CUI [1])
karnofsky status
Item
karnofsky status greater than or equal to 70%.
boolean
C0206065 (UMLS CUI [1])
life expectancy
Item
life expectancy of greater than 1 year.
boolean
C0023671 (UMLS CUI [1])
serum creatinine
Item
serum creatinine less than or equal to 1.5 mg/dl unless felt to be secondary to lymphoma.
boolean
C0201976 (UMLS CUI [1])
Bilirubin, SGOT/SGPT
Item
bilirubin less than or equal to 1.5 mg/dl unless felt to be secondary to lymphoma or gilbert's disease. sgot/sgpt less than or equal to 3.5 x upper limit of normal.
boolean
C1278039 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
C0201899 (UMLS CUI [2])
C0201836 (UMLS CUI [3])
informed consent
Item
ability to give informed consent. ability to return to clinic for adequate follow-up for the period that the protocol requires.
boolean
C0021430 (UMLS CUI [1])
the presence of any exclusion criteria
Item
the presence of any exclusion criteria (listed below) will prohibit entry onto study:
boolean
C0680251 (UMLS CUI [1])
irradiation
Item
prior total body irradiation.
boolean
C1522449 (UMLS CUI [1])
infectious process
Item
presence of antibodies to hiv or hepatitis b surface antigen or other active infectious process.
boolean
C0019682 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
C0019163 (UMLS CUI [2])
pregnancy
Item
pregnant or lactation. fertile men and women must plan to use an effective contraception. a beta-hcg level will be obtained in women of child-bearing potential.
boolean
C0032961 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
C0700589 (UMLS CUI [2])
malignancy
Item
patients with previous or concomitant malignancy, regardless of site, except curatively treated squamous or basal cell carcinoma of the skin, or effectively treated carcinoma in situ of the cervix.
boolean
C0006826 (UMLS CUI [1])
informed consent
Item
patient unwilling to give informed consent.
boolean
C0021430 (UMLS CUI [1])
any medical or psychiatric condition that in the opinion of the protocol chairman would compromise the patient's ability to tolerate this treatment.
Item
any medical or psychiatric condition that in the opinion of the protocol chairman would compromise the patient's ability to tolerate this treatment.
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
cns lymphoma
Item
patients with cns lymphoma (current or previously treated) will not be eligible.
boolean
C0280803 (UMLS CUI [1])