ID

16451

Descripción

Randomized Controlled Phase II Trial of Pre-operative Celecoxib Treatment in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01695226

Link

https://clinicaltrials.gov/show/NCT01695226

Palabras clave

Versiones (1)
  1. 17/7/16 17/7/16 -
Subido en

17 de julio de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT01695226

Inglés

Eligibility Breast Neoplasms NCT01695226

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
female patients suspected of having invasive breast cancer, >1 cm in diameter, and in whom there is an indication for a core or incision biopsy
Descripción

invasive breast cancer, indication for biopsy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0853879
UMLS CUI [2,1]
C0392360
UMLS CUI [2,2]
C0405352
age <75 years at time of diagnosis
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
patient willing and able to comply with the study prescriptions
Descripción

Compliance

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1321605
patient able to give written informed consent before patient registration/randomisation
Descripción

Written consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
pre- and post-menopausal patients are eligible
Descripción

Menopausal state

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0025320
hormone receptor positive and negative patients are eligible
Descripción

Hormone receptor status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1562029
UMLS CUI [2]
C2584453
a negative pregnancy test in pre-menopausal women
Descripción

a negative pregnancy test in pre-menopausal women

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0427780
UMLS CUI [1,2]
C0232969
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
hiv, hbv or hcv positivity
Descripción

hiv, hbv or hcv positivity

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019699
UMLS CUI [2]
C0856706
UMLS CUI [3]
C1112419
known hypersensitivity to nsaids
Descripción

hypersensitivity to nsaids

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0003211
a history of upper gastro-intestinal bleeding
Descripción

upper gastro-intestinal bleeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0041909
endoscopically proven upper gastro-intestinal ulceration
Descripción

upper gastro-intestinal ulceration

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030920
UMLS CUI [1,2]
C3203348
patients using nsaids, including salicyclic acid
Descripción

nsaids

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003211
systemic use of corticosteroids
Descripción

systemic corticosteroids

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2825233
a history or the presence of any other malignancy excepting adequately treated squamous cell skin cancer or in situ carcinoma of the cervix
Descripción

other malignancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0009488
patients who have been treated with neo-adjuvant chemotherapy or hormone therapy
Descripción

neo-adjuvant chemotherapy or hormone therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3665472
UMLS CUI [1,2]
C0600558
UMLS CUI [2]
C0279025
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Similar models

Eligibility Breast Neoplasms NCT01695226

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
invasive breast cancer, indication for biopsy
Item
female patients suspected of having invasive breast cancer, >1 cm in diameter, and in whom there is an indication for a core or incision biopsy
boolean
C0853879 (UMLS CUI [1])
C0392360 (UMLS CUI [2,1])
C0405352 (UMLS CUI [2,2])
Age
Item
age <75 years at time of diagnosis
boolean
C0001779 (UMLS CUI [1])
Compliance
Item
patient willing and able to comply with the study prescriptions
boolean
C1321605 (UMLS CUI [1])
Written consent
Item
patient able to give written informed consent before patient registration/randomisation
boolean
C0021430 (UMLS CUI [1])
Menopausal state
Item
pre- and post-menopausal patients are eligible
boolean
C0025320 (UMLS CUI [1])
Hormone receptor status
Item
hormone receptor positive and negative patients are eligible
boolean
C1562029 (UMLS CUI [1])
C2584453 (UMLS CUI [2])
a negative pregnancy test in pre-menopausal women
Item
a negative pregnancy test in pre-menopausal women
boolean
C0427780 (UMLS CUI [1,1])
C0232969 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
hiv, hbv or hcv positivity
Item
hiv, hbv or hcv positivity
boolean
C0019699 (UMLS CUI [1])
C0856706 (UMLS CUI [2])
C1112419 (UMLS CUI [3])
hypersensitivity to nsaids
Item
known hypersensitivity to nsaids
boolean
C0020517 (UMLS CUI [1,1])
C0003211 (UMLS CUI [1,2])
upper gastro-intestinal bleeding
Item
a history of upper gastro-intestinal bleeding
boolean
C0041909 (UMLS CUI [1])
upper gastro-intestinal ulceration
Item
endoscopically proven upper gastro-intestinal ulceration
boolean
C0030920 (UMLS CUI [1,1])
C3203348 (UMLS CUI [1,2])
nsaids
Item
patients using nsaids, including salicyclic acid
boolean
C0003211 (UMLS CUI [1])
systemic corticosteroids
Item
systemic use of corticosteroids
boolean
C2825233 (UMLS CUI [1])
other malignancy
Item
a history or the presence of any other malignancy excepting adequately treated squamous cell skin cancer or in situ carcinoma of the cervix
boolean
C0006826 (UMLS CUI [1])
C0009488 (UMLS CUI [2])
neo-adjuvant chemotherapy or hormone therapy
Item
patients who have been treated with neo-adjuvant chemotherapy or hormone therapy
boolean
C3665472 (UMLS CUI [1,1])
C0600558 (UMLS CUI [1,2])
C0279025 (UMLS CUI [2])
Volver a la parte superior de la página 

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