ID

22397

Descripción

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

Link

https://clinicaltrials.gov/show/NCT00592501

Palabras clave

  1. 1/6/17 1/6/17 -
Subido en

1 de junio de 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Nasopharyngeal Carcinoma NCT00592501

Eligibility Nasopharyngeal Carcinoma NCT00592501

Inclusion Criteria
Descripción

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.
Descripción

squamous cell carcinoma of the nasopharynx, TNM stage

Tipo de datos

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.
Descripción

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

Tipo de datos

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.
Descripción

zubrod performance status, karnofsky

Tipo de datos

boolean

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

pre-treatment evaluation of tumor extent and tumor measurement

Tipo de datos

boolean

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

nutritional and general physical condition, chemoradiotherapy

Tipo de datos

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.
Descripción

renal function, platelet function

Tipo de datos

boolean

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

age

Tipo de datos

boolean

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

alcohol addiction

Tipo de datos

boolean

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

women of childbearing potential, pregnancy test

Tipo de datos

boolean

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

Exclusion Criteria

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

tumor stage, distant metastases

Tipo de datos

boolean

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

prior radiotherapy, head and neck tumor

Tipo de datos

boolean

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

study subject participation status, experimental therapeutic cancer treatment

Tipo de datos

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.
Descripción

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

Tipo de datos

boolean

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

active infection

Tipo de datos

boolean

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

severe comorbidity

Tipo de datos

boolean

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

amifostine, pilocarpine

Tipo de datos

boolean

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

pregnancy, breast feeding

Tipo de datos

boolean

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

peripheral neuropathy, nci ctcae grade

Tipo de datos

boolean

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

altered hearing, nci ctcae grade

Tipo de datos

boolean

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

Similar models

Eligibility Nasopharyngeal Carcinoma NCT00592501

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial