ID

17738

Beschreibung

Capecitabine in Women With Operable Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00148720

Link

https://clinicaltrials.gov/show/NCT00148720

Stichworte

Versionen (1)
  1. 30.09.16 30.09.16 -
Hochgeladen am

30. September 2016

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Invasive Breast Carcinoma NCT00148720

Englisch

Eligibility Invasive Breast Carcinoma NCT00148720

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histological confirmation of primary invasive breast cancer
Beschreibung

Primary invasive malignant neoplasm of female breast

Datentyp

boolean

Alias
UMLS CUI [1]
C4076461
stage i-iii operable breast cancer.
Beschreibung

Breast Carcinoma Operable | TNM clinical staging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205188
UMLS CUI [2]
C3258246
primary tumor must be greater than or equal to 2cm by radiographic imaging or palpitation
Beschreibung

primary tumor size | Radiographic imaging | Palpation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0677930
UMLS CUI [1,2]
C0456389
UMLS CUI [2]
C0457276
UMLS CUI [3]
C0030247
women greater than 18 years of age
Beschreibung

Gender | Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
ecog performance status 0-1
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
wbc > 4000/mm3
Beschreibung

White Blood Cell Count procedure

Datentyp

boolean

Alias
UMLS CUI [1]
C0023508
platelet count > 100,000/mm3
Beschreibung

Platelet Count measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0032181
sgot < 2x uln
Beschreibung

Aspartate aminotransferase measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0201899
calculated creatinine clearance > 50ml/min
Beschreibung

Creatinine clearance measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0373595
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
evidence of metastatic (stage iv) cancer on physical exam or any diagnostic study.
Beschreibung

Neoplasm Metastasis Evidence of | Carcinoma breast stage IV | Physical Examination | Diagnostic tests

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0332120
UMLS CUI [2]
C0278488
UMLS CUI [3]
C0031809
UMLS CUI [4]
C0086143
pregnant or breast-feeding women
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
inflammatory breast cancer
Beschreibung

Inflammatory Breast Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1]
C0278601
her2 positive disease
Beschreibung

HER2-positive carcinoma of breast

Datentyp

boolean

Alias
UMLS CUI [1]
C1960398
history of hypersensitivity to a 5-fu or known dihydropyrimidine dehydrogenase (dpd) deficiency
Beschreibung

Hypersensitivity Fluorouracil | Dihydropyrimidine Dehydrogenase Deficiency

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0016360
UMLS CUI [2]
C1959620
uncontrolled intercurrent illness
Beschreibung

Intercurrent disease Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0277557
UMLS CUI [1,2]
C0205318
prior history of breast cancer are ineligible except: diagnosed at least 2 years ago; present cancer is not in previously irradiated breast; no prior chemotherapy in the past 5 years; no prior high-dose chemotherapy with stem cell or bone marrow transplant.
Beschreibung

Breast Carcinoma Previous | irradiation of breast Previous | Prior Chemotherapy | Prior Chemotherapy High dose | Stem cell transplant | Bone Marrow Transplantation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205156
UMLS CUI [2,1]
C2148528
UMLS CUI [2,2]
C0205156
UMLS CUI [3]
C1514457
UMLS CUI [4,1]
C1514457
UMLS CUI [4,2]
C0444956
UMLS CUI [5]
C1504389
UMLS CUI [6]
C0005961
excisional biopsy performed prior to enrollment
Beschreibung

Excision biopsy

Datentyp

boolean

Alias
UMLS CUI [1]
C0184921
uncontrolled coagulopathy
Beschreibung

Blood Coagulation Disorder Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0205318
lack of physical integrity of the upper gastrointestinal tract or malabsorption syndrome.
Beschreibung

upper gastrointestinal tract Integrity Physical Lacking | Malabsorption Syndrome

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1268997
UMLS CUI [1,2]
C1947912
UMLS CUI [1,3]
C0205485
UMLS CUI [1,4]
C0332268
UMLS CUI [2]
C0024523
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Invasive Breast Carcinoma NCT00148720

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Primary invasive malignant neoplasm of female breast
Item
histological confirmation of primary invasive breast cancer
boolean
C4076461 (UMLS CUI [1])
Breast Carcinoma Operable | TNM clinical staging
Item
stage i-iii operable breast cancer.
boolean
C0678222 (UMLS CUI [1,1])
C0205188 (UMLS CUI [1,2])
C3258246 (UMLS CUI [2])
primary tumor size | Radiographic imaging | Palpation
Item
primary tumor must be greater than or equal to 2cm by radiographic imaging or palpitation
boolean
C0677930 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
C0457276 (UMLS CUI [2])
C0030247 (UMLS CUI [3])
Gender | Age
Item
women greater than 18 years of age
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
ECOG performance status
Item
ecog performance status 0-1
boolean
C1520224 (UMLS CUI [1])
White Blood Cell Count procedure
Item
wbc > 4000/mm3
boolean
C0023508 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count > 100,000/mm3
boolean
C0032181 (UMLS CUI [1])
Aspartate aminotransferase measurement
Item
sgot < 2x uln
boolean
C0201899 (UMLS CUI [1])
Creatinine clearance measurement
Item
calculated creatinine clearance > 50ml/min
boolean
C0373595 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Neoplasm Metastasis Evidence of | Carcinoma breast stage IV | Physical Examination | Diagnostic tests
Item
evidence of metastatic (stage iv) cancer on physical exam or any diagnostic study.
boolean
C0027627 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
C0278488 (UMLS CUI [2])
C0031809 (UMLS CUI [3])
C0086143 (UMLS CUI [4])
Pregnancy | Breast Feeding
Item
pregnant or breast-feeding women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Inflammatory Breast Carcinoma
Item
inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
HER2-positive carcinoma of breast
Item
her2 positive disease
boolean
C1960398 (UMLS CUI [1])
Hypersensitivity Fluorouracil | Dihydropyrimidine Dehydrogenase Deficiency
Item
history of hypersensitivity to a 5-fu or known dihydropyrimidine dehydrogenase (dpd) deficiency
boolean
C0020517 (UMLS CUI [1,1])
C0016360 (UMLS CUI [1,2])
C1959620 (UMLS CUI [2])
Intercurrent disease Uncontrolled
Item
uncontrolled intercurrent illness
boolean
C0277557 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Breast Carcinoma Previous | irradiation of breast Previous | Prior Chemotherapy | Prior Chemotherapy High dose | Stem cell transplant | Bone Marrow Transplantation
Item
prior history of breast cancer are ineligible except: diagnosed at least 2 years ago; present cancer is not in previously irradiated breast; no prior chemotherapy in the past 5 years; no prior high-dose chemotherapy with stem cell or bone marrow transplant.
boolean
C0678222 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C2148528 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C1514457 (UMLS CUI [3])
C1514457 (UMLS CUI [4,1])
C0444956 (UMLS CUI [4,2])
C1504389 (UMLS CUI [5])
C0005961 (UMLS CUI [6])
Excision biopsy
Item
excisional biopsy performed prior to enrollment
boolean
C0184921 (UMLS CUI [1])
Blood Coagulation Disorder Uncontrolled
Item
uncontrolled coagulopathy
boolean
C0005779 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
upper gastrointestinal tract Integrity Physical Lacking | Malabsorption Syndrome
Item
lack of physical integrity of the upper gastrointestinal tract or malabsorption syndrome.
boolean
C1268997 (UMLS CUI [1,1])
C1947912 (UMLS CUI [1,2])
C0205485 (UMLS CUI [1,3])
C0332268 (UMLS CUI [1,4])
C0024523 (UMLS CUI [2])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video