ID

38326

Description

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

Lien

https://clinicaltrials.gov/show/NCT01626950

Mots-clés

Versions (1)
  1. 10/10/2019 10/10/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

10 octobre 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT01626950

Anglais

Eligibility Breast Neoplasms NCT01626950

1 Formulaires  
Criteria
Description

Criteria

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

Informed Consent

Type de données

boolean

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

Patient Health insurance plan Affiliated | Patient Health insurance plan beneficiary

Type de données

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
Description

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

Type de données

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):
Description

Inclusion criteria | Control Group

Type de données

boolean

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

Informed Consent

Type de données

boolean

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

Patient Health insurance plan Affiliated | Patient Health insurance plan beneficiary

Type de données

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
Description

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

Type de données

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):
Description

Exclusion Criteria | Clinical Study Case | Control Group

Type de données

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
Description

Exclusion Clinical Trial Period

Type de données

boolean

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

Protection of patient Judicial aspects | Patient Guardianship

Type de données

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
Description

Pregnancy | Childbirth | Breast Feeding

Type de données

boolean

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

Study Subject Participation Status Refusal to Participate

Type de données

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
Description

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

Type de données

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
Description

Patient Information Unsuccessful

Type de données

boolean

Alias
UMLS CUI [1,1]
C1955348
UMLS CUI [1,2]
C1272705
Retour au début de la page

Similar models

Eligibility Breast Neoplasms NCT01626950

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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