ID

38321

Beschreibung

Randomized Phase II Trial of Anastrozole Plus Metronomic Tegafur-uracil as Neo-adjuvant Therapy in Postmenopausal Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01262274

Link

https://clinicaltrials.gov/show/NCT01262274

Stichworte

Versionen (1)
  1. 10.10.19 10.10.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

10. Oktober 2019

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 Breast Neoplasms NCT01262274

Englisch

Eligibility Breast Neoplasms NCT01262274

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically-confirmed diagnosis of invasive breast cancer
Beschreibung

Invasive carcinoma of breast

Datentyp

boolean

Alias
UMLS CUI [1]
C0853879
clinical stage t2, n0 or n1, m0 (tnm classification)
Beschreibung

TNM Breast tumor staging

Datentyp

boolean

Alias
UMLS CUI [1]
C0474926
patients must be postmenopausal
Beschreibung

Postmenopausal state

Datentyp

boolean

Alias
UMLS CUI [1]
C0232970
tumors are estrogen receptor (er) positive and human epidermal growth factor receptor (her2) negative
Beschreibung

Estrogen receptor positive tumor | Neoplasms HER2 Negative

Datentyp

boolean

Alias
UMLS CUI [1]
C1562312
UMLS CUI [2,1]
C0027651
UMLS CUI [2,2]
C2348908
ecog performance status (ps) 0 or 1
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
patients must be able to swallow tablets and capsules
Beschreibung

Able to swallow Tablets | Able to swallow Capsules

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2712086
UMLS CUI [1,2]
C0039225
UMLS CUI [2,1]
C2712086
UMLS CUI [2,2]
C0006935
candidates for mastectomy or breast-conserving surgery
Beschreibung

Patients Appropriate Mastectomy | Patients Appropriate Breast-Conserving Surgery

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548787
UMLS CUI [1,3]
C0024881
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C1548787
UMLS CUI [2,3]
C0917927
adequate bone marrow, liver and renal function
Beschreibung

Bone Marrow function | Liver function | Renal function

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0005953
UMLS CUI [1,2]
C0031843
UMLS CUI [2]
C0232741
UMLS CUI [3]
C0232804
written informed consent was obtained from all patients before randomization.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
inoperable, bilateral or inflammatory breast cancer
Beschreibung

Breast Carcinoma Inoperable | Bilateral breast cancer | Inflammatory Breast Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205187
UMLS CUI [2]
C0281267
UMLS CUI [3]
C0278601
multiple carcinoma
Beschreibung

Multiple malignancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0346429
personal history of invasive carcinoma
Beschreibung

Invasive Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1]
C1334274
patients receive systemic therapy of corticosteroid
Beschreibung

Systemic Corticosteroid Therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C4053960
patients receive estrogen preparation or raloxifene
Beschreibung

Estrogens | Raloxifene

Datentyp

boolean

Alias
UMLS CUI [1]
C0014939
UMLS CUI [2]
C0244404
patients with other concurrent severe and/or uncontrolled medical disease
Beschreibung

Comorbidity Severe | Comorbidity Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0009488
UMLS CUI [2,2]
C0205318
patients whom doctors judged inadequate to the enrollment of this study by other reasons.
Beschreibung

Study Subject Participation Status Inadequate

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0205412
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Breast Neoplasms NCT01262274

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Invasive carcinoma of breast
Item
histologically-confirmed diagnosis of invasive breast cancer
boolean
C0853879 (UMLS CUI [1])
TNM Breast tumor staging
Item
clinical stage t2, n0 or n1, m0 (tnm classification)
boolean
C0474926 (UMLS CUI [1])
Postmenopausal state
Item
patients must be postmenopausal
boolean
C0232970 (UMLS CUI [1])
Estrogen receptor positive tumor | Neoplasms HER2 Negative
Item
tumors are estrogen receptor (er) positive and human epidermal growth factor receptor (her2) negative
boolean
C1562312 (UMLS CUI [1])
C0027651 (UMLS CUI [2,1])
C2348908 (UMLS CUI [2,2])
ECOG performance status
Item
ecog performance status (ps) 0 or 1
boolean
C1520224 (UMLS CUI [1])
Able to swallow Tablets | Able to swallow Capsules
Item
patients must be able to swallow tablets and capsules
boolean
C2712086 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
C2712086 (UMLS CUI [2,1])
C0006935 (UMLS CUI [2,2])
Patients Appropriate Mastectomy | Patients Appropriate Breast-Conserving Surgery
Item
candidates for mastectomy or breast-conserving surgery
boolean
C0030705 (UMLS CUI [1,1])
C1548787 (UMLS CUI [1,2])
C0024881 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C1548787 (UMLS CUI [2,2])
C0917927 (UMLS CUI [2,3])
Bone Marrow function | Liver function | Renal function
Item
adequate bone marrow, liver and renal function
boolean
C0005953 (UMLS CUI [1,1])
C0031843 (UMLS CUI [1,2])
C0232741 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
Informed Consent
Item
written informed consent was obtained from all patients before randomization.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Breast Carcinoma Inoperable | Bilateral breast cancer | Inflammatory Breast Carcinoma
Item
inoperable, bilateral or inflammatory breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C0281267 (UMLS CUI [2])
C0278601 (UMLS CUI [3])
Multiple malignancy
Item
multiple carcinoma
boolean
C0346429 (UMLS CUI [1])
Invasive Carcinoma
Item
personal history of invasive carcinoma
boolean
C1334274 (UMLS CUI [1])
Systemic Corticosteroid Therapy
Item
patients receive systemic therapy of corticosteroid
boolean
C4053960 (UMLS CUI [1])
Estrogens | Raloxifene
Item
patients receive estrogen preparation or raloxifene
boolean
C0014939 (UMLS CUI [1])
C0244404 (UMLS CUI [2])
Comorbidity Severe | Comorbidity Uncontrolled
Item
patients with other concurrent severe and/or uncontrolled medical disease
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0009488 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
Study Subject Participation Status Inadequate
Item
patients whom doctors judged inadequate to the enrollment of this study by other reasons.
boolean
C2348568 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
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