ID

13097

Beschrijving

Radiotherapy Versus Radiotherapy Plus Chemotherapy in Early Stage Follicular Lymphoma; ODM derived from: https://clinicaltrials.gov/show/NCT00115700

Link

https://clinicaltrials.gov/show/NCT00115700

Trefwoorden

Versies (1)
  1. 15-01-16 15-01-16 -
Geüploaded op

15 januari 2016

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Follicular Lymphoma NCT00115700

Engels

Eligibility Follicular Lymphoma NCT00115700

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients (≥ 18 years old) with histologically documented "follicular lymphoma, grade 1", grade 2", or "follicular lymphoma, grade 3a" diagnosed following an excisional, incisional or generous core biopsy. (i.e. an fna alone is insufficient.)
Beschrijving

age, follicular lymphoma grade, biopsy

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0024301
UMLS CUI [2,2]
C0005558
UMLS CUI [2,3]
C0919553
disease limited to stages i and ii after adequate staging
Beschrijving

disease stage

Datatype

boolean

Alias
UMLS CUI [1]
C0699749
anticipated life expectancy > 5 years
Beschrijving

life expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
given written informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
been assessed by a radiation oncologist and a medical oncologist/ haematologist
Beschrijving

assessment

Datatype

boolean

Alias
UMLS CUI [1]
C1516048
wcc > 3.0 x 10^9/l, platelet count > 100 x 10^9/l, serum creatinine < 0.15 mmol/l
Beschrijving

wbc, platelet count, creatinine

Datatype

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0201976
UMLS CUI [3]
C0032181
ability to commence radiotherapy within 6 weeks of randomisation
Beschrijving

radiotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C1321605
women using effective contraception, are not pregnant and agree not to become pregnant during participating in the trial and during the 12 months thereafter. men agree not to father a child during participation in the trial and during the 12 months thereafter.
Beschrijving

contraception, pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
UMLS CUI [2]
C0032961
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
received previous systemic cytotoxic chemotherapy.
Beschrijving

chemotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0392920
received previous radiotherapy, (except superficial radiation therapy for non-melanoma skin cancers).
Beschrijving

radiotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C1522449
received previous immunotherapy.
Beschrijving

immunotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0021083
a medical contraindication to radiotherapy, chemotherapy, or rituximab.
Beschrijving

contraindication

Datatype

boolean

Alias
UMLS CUI [1]
C1301624
any previous or concurrent malignancy other than curatively treated non-melanoma skin cancer, level 1 malignant melanoma, or in situ cervical cancer, unless disease and treatment-free for 5 years.
Beschrijving

malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
such extensive involvement of the thorax that treatment with radiation therapy alone would be hazardous because of excessive lung irradiation, even if a shrinking field technique were employed.
Beschrijving

thoracic involvement

Datatype

boolean

Alias
UMLS CUI [1,1]
C0817096
UMLS CUI [1,2]
C0449290
suspected or confirmed pregnancy. must not be lactating.
Beschrijving

pregnancy, lactation

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients who have known human immuno-deficiency virus (hiv) infection or active hepatitis b (hbv).
Beschrijving

hiv, hbv

Datatype

boolean

Alias
UMLS CUI [1]
C0019682
UMLS CUI [2]
C0019163
treatment within a clinical study within 30 days prior to study entry.
Beschrijving

study subject participation status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Follicular Lymphoma NCT00115700

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age, follicular lymphoma grade, biopsy
Item
adult patients (≥ 18 years old) with histologically documented "follicular lymphoma, grade 1", grade 2", or "follicular lymphoma, grade 3a" diagnosed following an excisional, incisional or generous core biopsy. (i.e. an fna alone is insufficient.)
boolean
C0001779 (UMLS CUI [1])
C0024301 (UMLS CUI [2,1])
C0005558 (UMLS CUI [2,2])
C0919553 (UMLS CUI [2,3])
disease stage
Item
disease limited to stages i and ii after adequate staging
boolean
C0699749 (UMLS CUI [1])
life expectancy
Item
anticipated life expectancy > 5 years
boolean
C0023671 (UMLS CUI [1])
informed consent
Item
given written informed consent
boolean
C0021430 (UMLS CUI [1])
assessment
Item
been assessed by a radiation oncologist and a medical oncologist/ haematologist
boolean
C1516048 (UMLS CUI [1])
wbc, platelet count, creatinine
Item
wcc > 3.0 x 10^9/l, platelet count > 100 x 10^9/l, serum creatinine < 0.15 mmol/l
boolean
C0023508 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0032181 (UMLS CUI [3])
radiotherapy
Item
ability to commence radiotherapy within 6 weeks of randomisation
boolean
C1522449 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
contraception, pregnancy
Item
women using effective contraception, are not pregnant and agree not to become pregnant during participating in the trial and during the 12 months thereafter. men agree not to father a child during participation in the trial and during the 12 months thereafter.
boolean
C0700589 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
chemotherapy
Item
received previous systemic cytotoxic chemotherapy.
boolean
C0392920 (UMLS CUI [1])
radiotherapy
Item
received previous radiotherapy, (except superficial radiation therapy for non-melanoma skin cancers).
boolean
C1522449 (UMLS CUI [1])
immunotherapy
Item
received previous immunotherapy.
boolean
C0021083 (UMLS CUI [1])
contraindication
Item
a medical contraindication to radiotherapy, chemotherapy, or rituximab.
boolean
C1301624 (UMLS CUI [1])
malignancy
Item
any previous or concurrent malignancy other than curatively treated non-melanoma skin cancer, level 1 malignant melanoma, or in situ cervical cancer, unless disease and treatment-free for 5 years.
boolean
C0006826 (UMLS CUI [1])
thoracic involvement
Item
such extensive involvement of the thorax that treatment with radiation therapy alone would be hazardous because of excessive lung irradiation, even if a shrinking field technique were employed.
boolean
C0817096 (UMLS CUI [1,1])
C0449290 (UMLS CUI [1,2])
pregnancy, lactation
Item
suspected or confirmed pregnancy. must not be lactating.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
hiv, hbv
Item
patients who have known human immuno-deficiency virus (hiv) infection or active hepatitis b (hbv).
boolean
C0019682 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
study subject participation status
Item
treatment within a clinical study within 30 days prior to study entry.
boolean
C2348568 (UMLS CUI [1])
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