ID

38363

Descripción

Fluorescence-guided Resection in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01110954

Link

https://clinicaltrials.gov/show/NCT01110954

Palabras clave

Versiones (1)
  1. 12/10/19 12/10/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

12 de octubre de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Tumour NCT01110954

Inglés

Eligibility Breast Tumour NCT01110954

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
written informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
caucasian female postmenopausal patients
Descripción

Caucasian | Gender | Postmenopausal state

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0043157
UMLS CUI [2]
C0079399
UMLS CUI [3]
C0232970
patients with histologically confirmed primary palpable and nonpalpable breast cancer sized up to 5 cm (t1 - t2)
Descripción

Breast Carcinoma Palpable TNM Breast tumor staging | Breast Carcinoma Non-Palpable TNM Breast tumor staging | Tumor size

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0522499
UMLS CUI [1,3]
C0474926
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C4086626
UMLS CUI [2,3]
C0474926
UMLS CUI [3]
C0475440
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
suspicious lymphogenic metastases (cn1-3)
Descripción

Neoplasm Metastasis Suspicious TNM clinical staging

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0750493
UMLS CUI [1,3]
C3258246
acute or chronic hepatic diseases
Descripción

Liver disease | Chronic liver disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0341439
manifest renal diseases with renal dysfunction
Descripción

Kidney Disease | Renal dysfunction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0022658
UMLS CUI [2]
C3279454
relevant cardiac disease
Descripción

Heart Disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018799
preceding therapy of breast tumour under investigation
Descripción

Investigational Therapy Breast Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0949266
UMLS CUI [1,2]
C0678222
patients with multiple attempts of hook-wire placement in preparation of surgery
Descripción

Hooked wire Placement Attempt

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0441180
UMLS CUI [1,2]
C0589567
UMLS CUI [1,3]
C1516084
dementia or psychic condition that might interfere with the ability to understand the study and thus give a written informed consent
Descripción

Dementia Interferes with Comprehension Study Protocol | Mental condition Interferes with Comprehension Study Protocol | Dementia Interferes with Informed Consent | Mental condition Interferes with Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0497327
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0162340
UMLS CUI [1,4]
C2348563
UMLS CUI [2,1]
C3840291
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0162340
UMLS CUI [2,4]
C2348563
UMLS CUI [3,1]
C0497327
UMLS CUI [3,2]
C0521102
UMLS CUI [3,3]
C0021430
UMLS CUI [4,1]
C3840291
UMLS CUI [4,2]
C0521102
UMLS CUI [4,3]
C0021430
simultaneous participation in another clinical study or participation in another clinical study in the 30 days directly preceding treatment
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Breast Tumour NCT01110954

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Caucasian | Gender | Postmenopausal state
Item
caucasian female postmenopausal patients
boolean
C0043157 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
Breast Carcinoma Palpable TNM Breast tumor staging | Breast Carcinoma Non-Palpable TNM Breast tumor staging | Tumor size
Item
patients with histologically confirmed primary palpable and nonpalpable breast cancer sized up to 5 cm (t1 - t2)
boolean
C0678222 (UMLS CUI [1,1])
C0522499 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
C0678222 (UMLS CUI [2,1])
C4086626 (UMLS CUI [2,2])
C0474926 (UMLS CUI [2,3])
C0475440 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Neoplasm Metastasis Suspicious TNM clinical staging
Item
suspicious lymphogenic metastases (cn1-3)
boolean
C0027627 (UMLS CUI [1,1])
C0750493 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
Liver disease | Chronic liver disease
Item
acute or chronic hepatic diseases
boolean
C0023895 (UMLS CUI [1])
C0341439 (UMLS CUI [2])
Kidney Disease | Renal dysfunction
Item
manifest renal diseases with renal dysfunction
boolean
C0022658 (UMLS CUI [1])
C3279454 (UMLS CUI [2])
Heart Disease
Item
relevant cardiac disease
boolean
C0018799 (UMLS CUI [1])
Investigational Therapy Breast Carcinoma
Item
preceding therapy of breast tumour under investigation
boolean
C0949266 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Hooked wire Placement Attempt
Item
patients with multiple attempts of hook-wire placement in preparation of surgery
boolean
C0441180 (UMLS CUI [1,1])
C0589567 (UMLS CUI [1,2])
C1516084 (UMLS CUI [1,3])
Dementia Interferes with Comprehension Study Protocol | Mental condition Interferes with Comprehension Study Protocol | Dementia Interferes with Informed Consent | Mental condition Interferes with Informed Consent
Item
dementia or psychic condition that might interfere with the ability to understand the study and thus give a written informed consent
boolean
C0497327 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0162340 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
C3840291 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C2348563 (UMLS CUI [2,4])
C0497327 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0021430 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C0021430 (UMLS CUI [4,3])
Study Subject Participation Status
Item
simultaneous participation in another clinical study or participation in another clinical study in the 30 days directly preceding treatment
boolean
C2348568 (UMLS CUI [1])
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