ID

26568

Description

Intraoperative Gamma Camera for Breast Cancer Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT00757302

Lien

https://clinicaltrials.gov/show/NCT00757302

Mots-clés

Versions (1)
  1. 19/10/2017 19/10/2017 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

19 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00757302

Anglais

Eligibility Breast Cancer NCT00757302

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient major at the time of breast surgery.
Description

Adult | Operation on breast

Type de données

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C3714726
patient affiliated with a social security.
Description

Social security recipient

Type de données

boolean

Alias
UMLS CUI [1]
C0682299
consent dated and signed by the investigator and the subject.
Description

Informed Consent | Informed Consent Investigator

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0035173
subject having been informed of the sentinel lymph node procedure during the visit prior to breast surgery.
Description

Patient Information Sentinel Lymph Node procedure | Patient Visit Before Operation on breast

Type de données

boolean

Alias
UMLS CUI [1,1]
C1955348
UMLS CUI [1,2]
C1522495
UMLS CUI [1,3]
C0184661
UMLS CUI [2,1]
C1512346
UMLS CUI [2,2]
C0332152
UMLS CUI [2,3]
C3714726
patient having a unifocal infiltrative breast cancer (less than 2 cm) diagnosed preoperatively by core biopsy or cytology.
Description

Invasive carcinoma of breast Unifocal Size | Core biopsy | Cytology

Type de données

boolean

Alias
UMLS CUI [1,1]
C0853879
UMLS CUI [1,2]
C0443337
UMLS CUI [1,3]
C0456389
UMLS CUI [2]
C1318309
UMLS CUI [3]
C1305671
patient having a ductal carcinoma in situ (dcis), diagnosed preoperatively by core biopsy or cytology.
Description

DCIS Core biopsy | DCIS Cytology

Type de données

boolean

Alias
UMLS CUI [1,1]
C0007124
UMLS CUI [1,2]
C1318309
UMLS CUI [2,1]
C0007124
UMLS CUI [2,2]
C1305671
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
refusal of the patient to be included in the study.
Description

Participation Clinical Trial Refused

Type de données

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1705116
pregnant patient or during breastfeeding.
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
none of the patients will have undergone chemotherapy, locoregional radiotherapy or prevalent axillary lymph node.
Description

Chemotherapy | Therapeutic radiology procedure Local-Regional | Prevalence Axillary lymph nodes

Type de données

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2,1]
C1522449
UMLS CUI [2,2]
C1947913
UMLS CUI [3,1]
C0220900
UMLS CUI [3,2]
C0729594
diagnosed safeguarding justice and trust.
Description

ID.10

Type de données

boolean

Alias
UMLS CUI [1]
C3846158
patient with a psychiatric disorder makes it impossible for the collection of informed consent-patient with tumors greater than 2 cm or multifocal.
Description

Mental disorders Informed Consent Unable | Tumor size | Multifocal tumor

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C0021430
UMLS CUI [1,3]
C1299582
UMLS CUI [2]
C0475440
UMLS CUI [3]
C1302461
prevalent axillary lymph node.
Description

Prevalence Axillary lymph nodes

Type de données

boolean

Alias
UMLS CUI [1,1]
C0220900
UMLS CUI [1,2]
C0729594
Retour au début de la page

Similar models

Eligibility Breast Cancer NCT00757302

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Operation on breast
Item
patient major at the time of breast surgery.
boolean
C0001675 (UMLS CUI [1])
C3714726 (UMLS CUI [2])
Social security recipient
Item
patient affiliated with a social security.
boolean
C0682299 (UMLS CUI [1])
Informed Consent | Informed Consent Investigator
Item
consent dated and signed by the investigator and the subject.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0035173 (UMLS CUI [2,2])
Patient Information Sentinel Lymph Node procedure | Patient Visit Before Operation on breast
Item
subject having been informed of the sentinel lymph node procedure during the visit prior to breast surgery.
boolean
C1955348 (UMLS CUI [1,1])
C1522495 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C1512346 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
C3714726 (UMLS CUI [2,3])
Invasive carcinoma of breast Unifocal Size | Core biopsy | Cytology
Item
patient having a unifocal infiltrative breast cancer (less than 2 cm) diagnosed preoperatively by core biopsy or cytology.
boolean
C0853879 (UMLS CUI [1,1])
C0443337 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
C1318309 (UMLS CUI [2])
C1305671 (UMLS CUI [3])
DCIS Core biopsy | DCIS Cytology
Item
patient having a ductal carcinoma in situ (dcis), diagnosed preoperatively by core biopsy or cytology.
boolean
C0007124 (UMLS CUI [1,1])
C1318309 (UMLS CUI [1,2])
C0007124 (UMLS CUI [2,1])
C1305671 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Participation Clinical Trial Refused
Item
refusal of the patient to be included in the study.
boolean
C0679823 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant patient or during breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Chemotherapy | Therapeutic radiology procedure Local-Regional | Prevalence Axillary lymph nodes
Item
none of the patients will have undergone chemotherapy, locoregional radiotherapy or prevalent axillary lymph node.
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2,1])
C1947913 (UMLS CUI [2,2])
C0220900 (UMLS CUI [3,1])
C0729594 (UMLS CUI [3,2])
ID.10
Item
diagnosed safeguarding justice and trust.
boolean
C3846158 (UMLS CUI [1])
Mental disorders Informed Consent Unable | Tumor size | Multifocal tumor
Item
patient with a psychiatric disorder makes it impossible for the collection of informed consent-patient with tumors greater than 2 cm or multifocal.
boolean
C0004936 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0475440 (UMLS CUI [2])
C1302461 (UMLS CUI [3])
Prevalence Axillary lymph nodes
Item
prevalent axillary lymph node.
boolean
C0220900 (UMLS CUI [1,1])
C0729594 (UMLS CUI [1,2])
Retour au début de la page 

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