ID

27311

Descripción

FDG-PET/CT for Simulation and Radiation Treatment Planning of Early Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01432002

Link

https://clinicaltrials.gov/show/NCT01432002

Palabras clave

Versiones (1)
  1. 7/11/17 7/11/17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

7 de noviembre de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Neoplasm NCT01432002

Inglés

Eligibility Breast Neoplasm NCT01432002

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed breast carcinoma
Descripción

Breast Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678222
clinical stage t1-2 n0 m0
Descripción

TNM Breast tumor staging

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0474926
age > 18 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
signed informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
who performance index 3
Descripción

WHO performance status scale

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1298650
premenopausal women without contraception
Descripción

Premenopausal state | Contraceptive methods Absent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232969
UMLS CUI [2,1]
C0700589
UMLS CUI [2,2]
C0332197
gestation
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
lactating
Descripción

Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006147
prior surgery or radiotherapy on the same breast
Descripción

Prior surgery Breast Same | Prior radiation therapy Breast Same

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0455610
UMLS CUI [1,2]
C0006141
UMLS CUI [1,3]
C0445247
UMLS CUI [2,1]
C0279134
UMLS CUI [2,2]
C0006141
UMLS CUI [2,3]
C0445247
unable to understand study participation
Descripción

Study Protocol Comprehension Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582
bilateral breast cancer
Descripción

Bilateral breast cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0281267
prior ct thorax-abdomen and breast mri within 4 months of interview
Descripción

CT of chest and abdomen | MRI of breast

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1630402
UMLS CUI [2]
C0344104
presence of electromechanical implant and/or body ferromagnetic material
Descripción

Implanted Medical Device | Ferromagnet Materials

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2828363
UMLS CUI [2,1]
C3178787
UMLS CUI [2,2]
C0520510
previous history of renal insufficiency requiring dialysis and/or hospitalisation
Descripción

Renal Insufficiency Requirement Dialysis | Renal Insufficiency Hospitalization Required

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0011946
UMLS CUI [2,1]
C1565489
UMLS CUI [2,2]
C1708385
ureum and/or creatinine within 2 weeks of interview above lab's reference limits
Descripción

Urea increased | Creatinine increased

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0856880
UMLS CUI [2]
C0151578
history of contrast allergy
Descripción

Contrast media allergy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0570562
hyperthyroidy
Descripción

Hyperthyroidism

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0020550
claustrophobia.
Descripción

Claustrophobia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0008909
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Similar models

Eligibility Breast Neoplasm NCT01432002

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma
Item
histologically confirmed breast carcinoma
boolean
C0678222 (UMLS CUI [1])
TNM Breast tumor staging
Item
clinical stage t1-2 n0 m0
boolean
C0474926 (UMLS CUI [1])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
WHO performance status scale
Item
who performance index 3
boolean
C1298650 (UMLS CUI [1])
Premenopausal state | Contraceptive methods Absent
Item
premenopausal women without contraception
boolean
C0232969 (UMLS CUI [1])
C0700589 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Pregnancy
Item
gestation
boolean
C0032961 (UMLS CUI [1])
Breast Feeding
Item
lactating
boolean
C0006147 (UMLS CUI [1])
Prior surgery Breast Same | Prior radiation therapy Breast Same
Item
prior surgery or radiotherapy on the same breast
boolean
C0455610 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
C0445247 (UMLS CUI [1,3])
C0279134 (UMLS CUI [2,1])
C0006141 (UMLS CUI [2,2])
C0445247 (UMLS CUI [2,3])
Study Protocol Comprehension Unable
Item
unable to understand study participation
boolean
C2348563 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Bilateral breast cancer
Item
bilateral breast cancer
boolean
C0281267 (UMLS CUI [1])
CT of chest and abdomen | MRI of breast
Item
prior ct thorax-abdomen and breast mri within 4 months of interview
boolean
C1630402 (UMLS CUI [1])
C0344104 (UMLS CUI [2])
Implanted Medical Device | Ferromagnet Materials
Item
presence of electromechanical implant and/or body ferromagnetic material
boolean
C2828363 (UMLS CUI [1])
C3178787 (UMLS CUI [2,1])
C0520510 (UMLS CUI [2,2])
Renal Insufficiency Requirement Dialysis | Renal Insufficiency Hospitalization Required
Item
previous history of renal insufficiency requiring dialysis and/or hospitalisation
boolean
C1565489 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0011946 (UMLS CUI [1,3])
C1565489 (UMLS CUI [2,1])
C1708385 (UMLS CUI [2,2])
Urea increased | Creatinine increased
Item
ureum and/or creatinine within 2 weeks of interview above lab's reference limits
boolean
C0856880 (UMLS CUI [1])
C0151578 (UMLS CUI [2])
Contrast media allergy
Item
history of contrast allergy
boolean
C0570562 (UMLS CUI [1])
Hyperthyroidism
Item
hyperthyroidy
boolean
C0020550 (UMLS CUI [1])
Claustrophobia
Item
claustrophobia.
boolean
C0008909 (UMLS CUI [1])
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