ID

30412

Descripción

Positron Emission Tomography Guided Therapy of Aggressive Non-Hodgkin's Lymphomas; ODM derived from: https://clinicaltrials.gov/show/NCT00554164

Link

https://clinicaltrials.gov/show/NCT00554164

Palabras clave

Versiones (1)
  1. 3/6/18 3/6/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

3 de junio de 2018

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.

Volver a los comentarios del modelo
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 Lymphoma, High-grade NCT00554164

Inglés

Eligibility Lymphoma, High-grade NCT00554164

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
aggressive b-cell or t-cell non-hodgkin's lymphoma
Descripción

B-Cell Lymphoma Aggressive | T-Cell Lymphoma Aggressive

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0079731
UMLS CUI [1,2]
C0580822
UMLS CUI [2,1]
C0079772
UMLS CUI [2,2]
C0580822
pathological pre-treatment pet scan
Descripción

PET scan pre treatment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032743
UMLS CUI [1,2]
C2709094
performance status ecog 0-3
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
age 18 - 80 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
ability to understand the purpose of the study and act accordingly
Descripción

Comprehension Study Protocol | Protocol Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C0525058
willingness to use adequate contraception
Descripción

Contraceptive methods Willing

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0600109
informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
burkitt's lymphoma
Descripción

Burkitt Lymphoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006413
primary central nervous system lymphoma
Descripción

Primary central nervous system lymphoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0280803
previous chemo- and/or radiotherapy
Descripción

Prior Chemotherapy | Prior radiation therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2]
C0279134
other cancer within preceding 5 years
Descripción

Cancer Other

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1707251
hiv infection, active viral hepatitis or other uncontrolled infection
Descripción

HIV Infection | Viral hepatitis | Communicable Disease Uncontrolled

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0042721
UMLS CUI [3,1]
C0009450
UMLS CUI [3,2]
C0205318
other medical conditions precluding administration of planned therapy
Descripción

Other medical condition Excludes Planned Treatment

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C3641097
pregnancy or lactation
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
Volver a la parte superior de la página

Similar models

Eligibility Lymphoma, High-grade NCT00554164

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
B-Cell Lymphoma Aggressive | T-Cell Lymphoma Aggressive
Item
aggressive b-cell or t-cell non-hodgkin's lymphoma
boolean
C0079731 (UMLS CUI [1,1])
C0580822 (UMLS CUI [1,2])
C0079772 (UMLS CUI [2,1])
C0580822 (UMLS CUI [2,2])
PET scan pre treatment
Item
pathological pre-treatment pet scan
boolean
C0032743 (UMLS CUI [1,1])
C2709094 (UMLS CUI [1,2])
ECOG performance status
Item
performance status ecog 0-3
boolean
C1520224 (UMLS CUI [1])
Age
Item
age 18 - 80 years
boolean
C0001779 (UMLS CUI [1])
Comprehension Study Protocol | Protocol Compliance
Item
ability to understand the purpose of the study and act accordingly
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Contraceptive methods Willing
Item
willingness to use adequate contraception
boolean
C0700589 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Burkitt Lymphoma
Item
burkitt's lymphoma
boolean
C0006413 (UMLS CUI [1])
Primary central nervous system lymphoma
Item
primary central nervous system lymphoma
boolean
C0280803 (UMLS CUI [1])
Prior Chemotherapy | Prior radiation therapy
Item
previous chemo- and/or radiotherapy
boolean
C1514457 (UMLS CUI [1])
C0279134 (UMLS CUI [2])
Cancer Other
Item
other cancer within preceding 5 years
boolean
C1707251 (UMLS CUI [1])
HIV Infection | Viral hepatitis | Communicable Disease Uncontrolled
Item
hiv infection, active viral hepatitis or other uncontrolled infection
boolean
C0019693 (UMLS CUI [1])
C0042721 (UMLS CUI [2])
C0009450 (UMLS CUI [3,1])
C0205318 (UMLS CUI [3,2])
Other medical condition Excludes Planned Treatment
Item
other medical conditions precluding administration of planned therapy
boolean
C3843040 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C3641097 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

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