ID

38326

Descripción

Living Conditions and Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01626950

Link

https://clinicaltrials.gov/show/NCT01626950

Palabras clave

Versiones (1)
  1. 10/10/19 10/10/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

10 de octubre de 2019

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 Breast Neoplasms NCT01626950

Inglés

Eligibility Breast Neoplasms NCT01626950

1 formularios  
Criteria
Descripción

Criteria

patient has been correctly informed about the study, and agrees to participate
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
the patient must be insured or beneficiary of a health insurance plan
Descripción

Patient Health insurance plan Affiliated | Patient Health insurance plan beneficiary

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0679933
UMLS CUI [1,3]
C1510826
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0679933
UMLS CUI [2,3]
C1550502
incident breast cancer cases (diagnosis based on pathology) excluding sarcoma, classifiable as stage iii-iv, surgical cases
Descripción

Breast Carcinoma | Exception Sarcoma TNM clinical staging | Exception Operative Surgical Procedures

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C1261473
UMLS CUI [2,3]
C3258246
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0543467
inclusion criteria (for controls):
Descripción

Inclusion criteria | Control Group

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1512693
UMLS CUI [2]
C0009932
patient has been correctly informed about the study, and agrees to participate
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
the patient must be insured or beneficiary of a health insurance plan
Descripción

Patient Health insurance plan Affiliated | Patient Health insurance plan beneficiary

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0679933
UMLS CUI [1,3]
C1510826
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0679933
UMLS CUI [2,3]
C1550502
incident breast cancer cases (diagnosis based on pathology) excluding sarcoma, classifiable as stage i-ii, surgical cases
Descripción

Breast Carcinoma | Exception Sarcoma TNM clinical staging | Exception Operative Surgical Procedures

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C1261473
UMLS CUI [2,3]
C3258246
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0543467
exclusion criteria (for cases and controls):
Descripción

Exclusion Criteria | Clinical Study Case | Control Group

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2]
C1706256
UMLS CUI [3]
C0009932
the patient is in an exclusion period determined by a previous study
Descripción

Exclusion Clinical Trial Period

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C2347804
the patient is under judicial protection, under tutorship or curatorship
Descripción

Protection of patient Judicial aspects | Patient Guardianship

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0412786
UMLS CUI [1,2]
C0243116
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0870627
the patient is pregnant, parturient, or breastfeeding
Descripción

Pregnancy | Childbirth | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C1148523
UMLS CUI [3]
C0006147
the patient is opposed to study participation
Descripción

Study Subject Participation Status Refusal to Participate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1136454
women not able to answer a questionnaire due to language barriers or due to vascular or degenerative cerebral dysfunction
Descripción

Gender | Questionnaire Completion Unable | Language Barriers | Cerebral dysfunction Vascular | Cerebral dysfunction Degenerative

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0034394
UMLS CUI [2,2]
C0205197
UMLS CUI [2,3]
C1299582
UMLS CUI [3]
C0237167
UMLS CUI [4,1]
C0262405
UMLS CUI [4,2]
C1801960
UMLS CUI [5,1]
C0262405
UMLS CUI [5,2]
C1285162
it is impossible to correctly inform the patient
Descripción

Patient Information Unsuccessful

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1955348
UMLS CUI [1,2]
C1272705
Volver a la parte superior de la página

Similar models

Eligibility Breast Neoplasms NCT01626950

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Informed Consent
Item
patient has been correctly informed about the study, and agrees to participate
boolean
C0021430 (UMLS CUI [1])
Patient Health insurance plan Affiliated | Patient Health insurance plan beneficiary
Item
the patient must be insured or beneficiary of a health insurance plan
boolean
C0030705 (UMLS CUI [1,1])
C0679933 (UMLS CUI [1,2])
C1510826 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0679933 (UMLS CUI [2,2])
C1550502 (UMLS CUI [2,3])
Breast Carcinoma | Exception Sarcoma TNM clinical staging | Exception Operative Surgical Procedures
Item
incident breast cancer cases (diagnosis based on pathology) excluding sarcoma, classifiable as stage iii-iv, surgical cases
boolean
C0678222 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C1261473 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0543467 (UMLS CUI [3,2])
Inclusion criteria | Control Group
Item
inclusion criteria (for controls):
boolean
C1512693 (UMLS CUI [1])
C0009932 (UMLS CUI [2])
Informed Consent
Item
patient has been correctly informed about the study, and agrees to participate
boolean
C0021430 (UMLS CUI [1])
Patient Health insurance plan Affiliated | Patient Health insurance plan beneficiary
Item
the patient must be insured or beneficiary of a health insurance plan
boolean
C0030705 (UMLS CUI [1,1])
C0679933 (UMLS CUI [1,2])
C1510826 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C0679933 (UMLS CUI [2,2])
C1550502 (UMLS CUI [2,3])
Breast Carcinoma | Exception Sarcoma TNM clinical staging | Exception Operative Surgical Procedures
Item
incident breast cancer cases (diagnosis based on pathology) excluding sarcoma, classifiable as stage i-ii, surgical cases
boolean
C0678222 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C1261473 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0543467 (UMLS CUI [3,2])
Exclusion Criteria | Clinical Study Case | Control Group
Item
exclusion criteria (for cases and controls):
boolean
C0680251 (UMLS CUI [1])
C1706256 (UMLS CUI [2])
C0009932 (UMLS CUI [3])
Exclusion Clinical Trial Period
Item
the patient is in an exclusion period determined by a previous study
boolean
C2828389 (UMLS CUI [1,1])
C2347804 (UMLS CUI [1,2])
Protection of patient Judicial aspects | Patient Guardianship
Item
the patient is under judicial protection, under tutorship or curatorship
boolean
C0412786 (UMLS CUI [1,1])
C0243116 (UMLS CUI [1,2])
C0030705 (UMLS CUI [2,1])
C0870627 (UMLS CUI [2,2])
Pregnancy | Childbirth | Breast Feeding
Item
the patient is pregnant, parturient, or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C1148523 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Study Subject Participation Status Refusal to Participate
Item
the patient is opposed to study participation
boolean
C2348568 (UMLS CUI [1,1])
C1136454 (UMLS CUI [1,2])
Gender | Questionnaire Completion Unable | Language Barriers | Cerebral dysfunction Vascular | Cerebral dysfunction Degenerative
Item
women not able to answer a questionnaire due to language barriers or due to vascular or degenerative cerebral dysfunction
boolean
C0079399 (UMLS CUI [1])
C0034394 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0237167 (UMLS CUI [3])
C0262405 (UMLS CUI [4,1])
C1801960 (UMLS CUI [4,2])
C0262405 (UMLS CUI [5,1])
C1285162 (UMLS CUI [5,2])
Patient Information Unsuccessful
Item
it is impossible to correctly inform the patient
boolean
C1955348 (UMLS CUI [1,1])
C1272705 (UMLS CUI [1,2])
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