ID

12925

Beskrivning

Axillary Dissection Based on the Histological Result of the Sentinel Node, in Patients With Breast Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT00970983

Länk

https://clinicaltrials.gov/show/NCT00970983

Nyckelord

  1. 2016-01-06 2016-01-06 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

6 januari 2016

DOI

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Licens

Creative Commons BY-NC 3.0

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Eligibility Breast Carcinoma NCT00970983

Eligibility Breast Carcinoma NCT00970983

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
age between 40 and 75 years.
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
clinical, mammographic or ultrasonographic diagnosis of a unicentric carcinoma with an ultrasonographic diameter of equal or less than 2.0 cm.
Beskrivning

unicentric carcinoma

Datatyp

boolean

Alias
UMLS CUI [1]
C0678222
although not a factor of exclusion, a breast scintigraphy using mdp-99m is recommended for accurate determination of possible multifocality or multicentricity of the tumor, as well as for the determination of possible bone metastasis.
Beskrivning

breast scintigraphy

Datatyp

boolean

Alias
UMLS CUI [1]
C0034606
axillary lymph nodes that cannot be palpated or that are not clinically suspicious for metastasis.
Beskrivning

axillary lymph nodes

Datatyp

boolean

Alias
UMLS CUI [1]
C0729594
no previously executed therapy (including biopsy) at any outside institution.
Beskrivning

no previously executed therapy (including biopsy) at any outside institution.

Datatyp

boolean

Alias
UMLS CUI [1]
C0087111
those patients with nonpalpable lesions will be subjected to preoperative radioactive occult lesion localization (roll) or stereotactic biopsy.
Beskrivning

those patients with nonpalpable lesions will be subjected to preoperative radioactive occult lesion localization (roll) or stereotactic biopsy.

Datatyp

boolean

Alias
UMLS CUI [1]
C1711202
adequate patient information and signature of the informed consent.
Beskrivning

adequate patient information and signature of the informed consent.

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
lesions diagnosed as non-infiltrating (in-situ) ductal or lobular carcinoma.
Beskrivning

lesions diagnosed as non-infiltrating (in-situ) ductal or lobular carcinoma

Datatyp

boolean

Alias
UMLS CUI [1]
C0332448
paget's disease.
Beskrivning

paget's disease

Datatyp

boolean

Alias
UMLS CUI [1]
C1704323
documented multicentricity and/or abundant multifocality of the neoplasm.
Beskrivning

documented multicentricity and/or abundant multifocality of the neoplasm.

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
clinically metastatic lymph nodes.
Beskrivning

metastatic lymph nodes

Datatyp

boolean

Alias
UMLS CUI [1]
C0686619
patients previously biopsied at other institutions.
Beskrivning

patients previously biopsied at other institutions

Datatyp

boolean

Alias
UMLS CUI [1]
C0005558
carcinomas detected during pregnancy or lactation.
Beskrivning

carcinomas detected during pregnancy or lactation.

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
histotypes diverse from breast carcinoma lesions.
Beskrivning

histotypes diverse from breast carcinoma lesions

Datatyp

boolean

Alias
UMLS CUI [1]
C0019638
history of previous malignancy (excluding basocellular carcinoma, in-situ cervical carcinoma and/or contralateral breast carcinoma without recurrence for at least 15 years of follow-up).
Beskrivning

history of previous malignancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826

Similar models

Eligibility Breast Carcinoma NCT00970983

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age between 40 and 75 years.
boolean
C0001779 (UMLS CUI [1])
unicentric carcinoma
Item
clinical, mammographic or ultrasonographic diagnosis of a unicentric carcinoma with an ultrasonographic diameter of equal or less than 2.0 cm.
boolean
C0678222 (UMLS CUI [1])
breast scintigraphy
Item
although not a factor of exclusion, a breast scintigraphy using mdp-99m is recommended for accurate determination of possible multifocality or multicentricity of the tumor, as well as for the determination of possible bone metastasis.
boolean
C0034606 (UMLS CUI [1])
axillary lymph nodes
Item
axillary lymph nodes that cannot be palpated or that are not clinically suspicious for metastasis.
boolean
C0729594 (UMLS CUI [1])
no previously executed therapy (including biopsy) at any outside institution.
Item
no previously executed therapy (including biopsy) at any outside institution.
boolean
C0087111 (UMLS CUI [1])
those patients with nonpalpable lesions will be subjected to preoperative radioactive occult lesion localization (roll) or stereotactic biopsy.
Item
those patients with nonpalpable lesions will be subjected to preoperative radioactive occult lesion localization (roll) or stereotactic biopsy.
boolean
C1711202 (UMLS CUI [1])
adequate patient information and signature of the informed consent.
Item
adequate patient information and signature of the informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
lesions diagnosed as non-infiltrating (in-situ) ductal or lobular carcinoma
Item
lesions diagnosed as non-infiltrating (in-situ) ductal or lobular carcinoma.
boolean
C0332448 (UMLS CUI [1])
paget's disease
Item
paget's disease.
boolean
C1704323 (UMLS CUI [1])
documented multicentricity and/or abundant multifocality of the neoplasm.
Item
documented multicentricity and/or abundant multifocality of the neoplasm.
boolean
C0006826 (UMLS CUI [1])
metastatic lymph nodes
Item
clinically metastatic lymph nodes.
boolean
C0686619 (UMLS CUI [1])
patients previously biopsied at other institutions
Item
patients previously biopsied at other institutions.
boolean
C0005558 (UMLS CUI [1])
carcinomas detected during pregnancy or lactation.
Item
carcinomas detected during pregnancy or lactation.
boolean
C0032961 (UMLS CUI [1])
histotypes diverse from breast carcinoma lesions
Item
histotypes diverse from breast carcinoma lesions.
boolean
C0019638 (UMLS CUI [1])
history of previous malignancy
Item
history of previous malignancy (excluding basocellular carcinoma, in-situ cervical carcinoma and/or contralateral breast carcinoma without recurrence for at least 15 years of follow-up).
boolean
C0006826 (UMLS CUI [1])

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