ID

19553

Beschreibung

Randomized Phase II Trial Induction Therapy for Early Stage Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00209092

Link

https://clinicaltrials.gov/show/NCT00209092

Stichworte

  1. 10.01.17 10.01.17 -
Hochgeladen am

10. Januar 2017

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.

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 Cancer NCT00209092

Eligibility Breast Cancer NCT00209092

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically or cytologically confirmed breast carcinoma.
Beschreibung

Breast Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1]
C0678222
early stage breast cancer (stage 1, 2, 3).
Beschreibung

Early-Stage Breast Carcinoma TNM clinical staging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2986665
UMLS CUI [1,2]
C3258246
no evidence of disease outside the breast or chest wall, except ipsilateral axillary lymph nodes.
Beschreibung

Disease Breast outside Evidence | Disease chest wall outside Evidence | Disease Axillary lymph nodes Ipsilateral

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0006141
UMLS CUI [1,3]
C0205101
UMLS CUI [1,4]
C3887511
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C1279035
UMLS CUI [2,3]
C0205101
UMLS CUI [2,4]
C3887511
UMLS CUI [3,1]
C0012634
UMLS CUI [3,2]
C0729594
UMLS CUI [3,3]
C0441989
18 years of age or older.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
Beschreibung

Eligibility Determination Research Personnel

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013893
UMLS CUI [1,2]
C0035173
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior chemotherapy, hormonal therapy, biologic therapy or radiation therapy for breast cancer.
Beschreibung

Chemotherapy Breast Carcinoma | Hormone Therapy Breast Carcinoma | Biological treatment Breast Carcinoma | Therapeutic radiology procedure Breast Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0678222
UMLS CUI [2,1]
C0279025
UMLS CUI [2,2]
C0678222
UMLS CUI [3,1]
C1531518
UMLS CUI [3,2]
C0678222
UMLS CUI [4,1]
C1522449
UMLS CUI [4,2]
C0678222
major surgery within 28 days of study entry.
Beschreibung

major surgery

Datentyp

boolean

Alias
UMLS CUI [1]
C0679637
evidence of central nervous system (cns) metastases.
Beschreibung

CNS metastases Evidence of

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0686377
UMLS CUI [1,2]
C0332120
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
Beschreibung

Eligibility Determination Research Personnel

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013893
UMLS CUI [1,2]
C0035173

Ähnliche Modelle

Eligibility Breast Cancer NCT00209092

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma
Item
histologically or cytologically confirmed breast carcinoma.
boolean
C0678222 (UMLS CUI [1])
Early-Stage Breast Carcinoma TNM clinical staging
Item
early stage breast cancer (stage 1, 2, 3).
boolean
C2986665 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Disease Breast outside Evidence | Disease chest wall outside Evidence | Disease Axillary lymph nodes Ipsilateral
Item
no evidence of disease outside the breast or chest wall, except ipsilateral axillary lymph nodes.
boolean
C0012634 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
C0205101 (UMLS CUI [1,3])
C3887511 (UMLS CUI [1,4])
C0012634 (UMLS CUI [2,1])
C1279035 (UMLS CUI [2,2])
C0205101 (UMLS CUI [2,3])
C3887511 (UMLS CUI [2,4])
C0012634 (UMLS CUI [3,1])
C0729594 (UMLS CUI [3,2])
C0441989 (UMLS CUI [3,3])
Age
Item
18 years of age or older.
boolean
C0001779 (UMLS CUI [1])
Eligibility Determination Research Personnel
Item
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
boolean
C0013893 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Chemotherapy Breast Carcinoma | Hormone Therapy Breast Carcinoma | Biological treatment Breast Carcinoma | Therapeutic radiology procedure Breast Carcinoma
Item
prior chemotherapy, hormonal therapy, biologic therapy or radiation therapy for breast cancer.
boolean
C0392920 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0279025 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C1531518 (UMLS CUI [3,1])
C0678222 (UMLS CUI [3,2])
C1522449 (UMLS CUI [4,1])
C0678222 (UMLS CUI [4,2])
major surgery
Item
major surgery within 28 days of study entry.
boolean
C0679637 (UMLS CUI [1])
CNS metastases Evidence of
Item
evidence of central nervous system (cns) metastases.
boolean
C0686377 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
Eligibility Determination Research Personnel
Item
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
boolean
C0013893 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

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