ID

22397

Beschrijving

Proton Radiotherapy With Chemotherapy for Nasopharyngeal Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00592501

Link

https://clinicaltrials.gov/show/NCT00592501

Trefwoorden

Versies (1)
  1. 01-06-17 01-06-17 -
Geüploaded op

1 juni 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Nasopharyngeal Carcinoma NCT00592501

Engels

Eligibility Nasopharyngeal Carcinoma NCT00592501

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
biopsy proven greater than or equal to t2b and/or node positive non-metastatic, squamous cell carcinoma of the nasopharynx, types who i-iii.
Beschrijving

squamous cell carcinoma of the nasopharynx, TNM stage

Datatype

boolean

Alias
UMLS CUI [1,1]
C0279698
UMLS CUI [1,2]
C0475284
no head and neck surgery of the primary tumor or lymph nodes except incisional or excisional biopsies.
Beschrijving

no head and neck surgery of the primary tumor or lymph nodes except incisional or excisional biopsies

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512343
UMLS CUI [1,2]
C0279698
UMLS CUI [1,3]
C0677930
UMLS CUI [1,4]
C0024204
UMLS CUI [2,1]
C0005558
UMLS CUI [2,2]
C0279698
zubrod performance status 0-1 or karnofsky 70 or above.
Beschrijving

zubrod performance status, karnofsky

Datatype

boolean

Alias
UMLS CUI [1]
C3714786
UMLS CUI [2]
C0206065
all patients must undergo pre-treatment evaluation of tumor extent and tumor measurement.
Beschrijving

pre-treatment evaluation of tumor extent and tumor measurement

Datatype

boolean

Alias
UMLS CUI [1]
C2924250
nutritional and general physical condition must be considered compatible with the proposed chemoradiation treatment
Beschrijving

nutritional and general physical condition, chemoradiotherapy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1142435
UMLS CUI [1,2]
C1608413
UMLS CUI [1,3]
C0436307
patients must have adequate platelet and renal function as outlined in protocol.
Beschrijving

renal function, platelet function

Datatype

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C1254881
18 years of age or above.
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
no active alcohol addiction.
Beschrijving

alcohol addiction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0038586
UMLS CUI [1,2]
C0001948
women of childbearing potential must have a negative pregnancy test.
Beschrijving

women of childbearing potential, pregnancy test

Datatype

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0032976
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
stage ivc or evidence of distant metastases
Beschrijving

tumor stage, distant metastases

Datatype

boolean

Alias
UMLS CUI [1,1]
C1300072
UMLS CUI [1,2]
C0475284
UMLS CUI [2]
C0027627
previous irradiation for head and neck tumor
Beschrijving

prior radiotherapy, head and neck tumor

Datatype

boolean

Alias
UMLS CUI [1,1]
C0279134
UMLS CUI [1,2]
C0018671
patient is on other experimental therapeutic cancer treatment
Beschrijving

study subject participation status, experimental therapeutic cancer treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0013230
other malignancy except non-melanoma skin cancer or carcinomas of head and neck origin and have been controlled for at least 5 years.
Beschrijving

malignancy, non-melanoma skin cancer, carcinomas of head and neck controlled

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C3281209
UMLS CUI [3,1]
C0018671
UMLS CUI [3,2]
C2911690
active untreated infection
Beschrijving

active infection

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205177
major medical or psychiatric illness
Beschrijving

severe comorbidity

Datatype

boolean

Alias
UMLS CUI [1,1]
C0205082
UMLS CUI [1,2]
C0009488
prophylactic use of amifostine or pilocarpine
Beschrijving

amifostine, pilocarpine

Datatype

boolean

Alias
UMLS CUI [1]
C0015020
UMLS CUI [2]
C0031923
pregnant or breast feeding women
Beschrijving

pregnancy, breast feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
symptomatic peripheral neuropathy of grade 2 or greater by nci ctcae
Beschrijving

peripheral neuropathy, nci ctcae grade

Datatype

boolean

Alias
UMLS CUI [1,1]
C0031117
UMLS CUI [1,2]
C3887242
symptomatic altered hearing > grade 2 by ctcae
Beschrijving

altered hearing, nci ctcae grade

Datatype

boolean

Alias
UMLS CUI [1,1]
C0260662
UMLS CUI [1,2]
C3887242
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Similar models

Eligibility Nasopharyngeal Carcinoma NCT00592501

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
squamous cell carcinoma of the nasopharynx, TNM stage
Item
biopsy proven greater than or equal to t2b and/or node positive non-metastatic, squamous cell carcinoma of the nasopharynx, types who i-iii.
boolean
C0279698 (UMLS CUI [1,1])
C0475284 (UMLS CUI [1,2])
no head and neck surgery of the primary tumor or lymph nodes except incisional or excisional biopsies
Item
no head and neck surgery of the primary tumor or lymph nodes except incisional or excisional biopsies.
boolean
C1512343 (UMLS CUI [1,1])
C0279698 (UMLS CUI [1,2])
C0677930 (UMLS CUI [1,3])
C0024204 (UMLS CUI [1,4])
C0005558 (UMLS CUI [2,1])
C0279698 (UMLS CUI [2,2])
zubrod performance status, karnofsky
Item
zubrod performance status 0-1 or karnofsky 70 or above.
boolean
C3714786 (UMLS CUI [1])
C0206065 (UMLS CUI [2])
pre-treatment evaluation of tumor extent and tumor measurement
Item
all patients must undergo pre-treatment evaluation of tumor extent and tumor measurement.
boolean
C2924250 (UMLS CUI [1])
nutritional and general physical condition, chemoradiotherapy
Item
nutritional and general physical condition must be considered compatible with the proposed chemoradiation treatment
boolean
C1142435 (UMLS CUI [1,1])
C1608413 (UMLS CUI [1,2])
C0436307 (UMLS CUI [1,3])
renal function, platelet function
Item
patients must have adequate platelet and renal function as outlined in protocol.
boolean
C0232804 (UMLS CUI [1])
C1254881 (UMLS CUI [2])
age
Item
18 years of age or above.
boolean
C0001779 (UMLS CUI [1])
alcohol addiction
Item
no active alcohol addiction.
boolean
C0038586 (UMLS CUI [1,1])
C0001948 (UMLS CUI [1,2])
women of childbearing potential, pregnancy test
Item
women of childbearing potential must have a negative pregnancy test.
boolean
C3831118 (UMLS CUI [1,1])
C0032976 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
tumor stage, distant metastases
Item
stage ivc or evidence of distant metastases
boolean
C1300072 (UMLS CUI [1,1])
C0475284 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2])
prior radiotherapy, head and neck tumor
Item
previous irradiation for head and neck tumor
boolean
C0279134 (UMLS CUI [1,1])
C0018671 (UMLS CUI [1,2])
study subject participation status, experimental therapeutic cancer treatment
Item
patient is on other experimental therapeutic cancer treatment
boolean
C2348568 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
malignancy, non-melanoma skin cancer, carcinomas of head and neck controlled
Item
other malignancy except non-melanoma skin cancer or carcinomas of head and neck origin and have been controlled for at least 5 years.
boolean
C0006826 (UMLS CUI [1])
C3281209 (UMLS CUI [2])
C0018671 (UMLS CUI [3,1])
C2911690 (UMLS CUI [3,2])
active infection
Item
active untreated infection
boolean
C0009450 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
severe comorbidity
Item
major medical or psychiatric illness
boolean
C0205082 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
amifostine, pilocarpine
Item
prophylactic use of amifostine or pilocarpine
boolean
C0015020 (UMLS CUI [1])
C0031923 (UMLS CUI [2])
pregnancy, breast feeding
Item
pregnant or breast feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
peripheral neuropathy, nci ctcae grade
Item
symptomatic peripheral neuropathy of grade 2 or greater by nci ctcae
boolean
C0031117 (UMLS CUI [1,1])
C3887242 (UMLS CUI [1,2])
altered hearing, nci ctcae grade
Item
symptomatic altered hearing > grade 2 by ctcae
boolean
C0260662 (UMLS CUI [1,1])
C3887242 (UMLS CUI [1,2])
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