ID

38017

Beschreibung

Trial of Neoadjuvant Endostar, Docetaxel and Epirubicin for Patients With Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01479036

Link

https://clinicaltrials.gov/show/NCT01479036

Stichworte

  1. 08.09.19 08.09.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

8. September 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.

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 NCT01479036

Eligibility Breast Cancer NCT01479036

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed invasive breast cancer (core needle biopsy for breast cancer diagnosis and fine needle aspiration for lymph node metastasis diagnosis)
Beschreibung

Invasive carcinoma of breast | Core needle biopsy Breast Carcinoma Diagnosis | Fine needle aspiration Secondary malignant neoplasm of lymph node Diagnosis

Datentyp

boolean

Alias
UMLS CUI [1]
C0853879
UMLS CUI [2,1]
C1318309
UMLS CUI [2,2]
C0678222
UMLS CUI [2,3]
C0011900
UMLS CUI [3,1]
C1510483
UMLS CUI [3,2]
C0686619
UMLS CUI [3,3]
C0011900
stage ⅱa-ⅲc
Beschreibung

TNM Breast tumor staging

Datentyp

boolean

Alias
UMLS CUI [1]
C0474926
age 18-70
Beschreibung

Age

Datentyp

boolean

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

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
no evidence of distant metastasis
Beschreibung

Distant metastasis Absent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1269798
UMLS CUI [1,2]
C0332197
no previous therapy
Beschreibung

Prior Therapy Absent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0332197
normal hematologic function
Beschreibung

Hematologic function

Datentyp

boolean

Alias
UMLS CUI [1]
C0221130
left ventricular ejection fraction greater than 50 percent
Beschreibung

Left ventricular ejection fraction

Datentyp

boolean

Alias
UMLS CUI [1]
C0428772
no abnormality of renal or liver function
Beschreibung

Abnormality Absent Renal function | Abnormality Absent Liver function

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1704258
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0232804
UMLS CUI [2,1]
C1704258
UMLS CUI [2,2]
C0332197
UMLS CUI [2,3]
C0232741
written informed consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
with allergic constitution or possible allergic reflection to drugs to be used in this study
Beschreibung

Constitution allergic | Allergic Reaction Possible Investigational New Drugs

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0683521
UMLS CUI [1,2]
C0700624
UMLS CUI [2,1]
C1527304
UMLS CUI [2,2]
C0332149
UMLS CUI [2,3]
C0013230
any concurrent uncontrolled medical or psychiatric disorder
Beschreibung

Comorbidity Uncontrolled | Mental disorder Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
UMLS CUI [2,1]
C0004936
UMLS CUI [2,2]
C0205318
history of severe heart diseases, including congestive heart failure, unstable angina, uncontrolled arrhythmia, myocardial infarction, uncontrolled high blood pressure, or heart valve disease.
Beschreibung

Heart Diseases Severe | Congestive heart failure | Angina, Unstable | Cardiac Arrhythmia Uncontrolled | Myocardial Infarction | Uncontrolled hypertension | Heart valve disease

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0018802
UMLS CUI [3]
C0002965
UMLS CUI [4,1]
C0003811
UMLS CUI [4,2]
C0205318
UMLS CUI [5]
C0027051
UMLS CUI [6]
C1868885
UMLS CUI [7]
C0018824
history of bleeding diathesis
Beschreibung

Bleeding tendency

Datentyp

boolean

Alias
UMLS CUI [1]
C1458140
being pregnant or nursing
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147

Ähnliche Modelle

Eligibility Breast Cancer NCT01479036

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Invasive carcinoma of breast | Core needle biopsy Breast Carcinoma Diagnosis | Fine needle aspiration Secondary malignant neoplasm of lymph node Diagnosis
Item
histologically confirmed invasive breast cancer (core needle biopsy for breast cancer diagnosis and fine needle aspiration for lymph node metastasis diagnosis)
boolean
C0853879 (UMLS CUI [1])
C1318309 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C0011900 (UMLS CUI [2,3])
C1510483 (UMLS CUI [3,1])
C0686619 (UMLS CUI [3,2])
C0011900 (UMLS CUI [3,3])
TNM Breast tumor staging
Item
stage ⅱa-ⅲc
boolean
C0474926 (UMLS CUI [1])
Age
Item
age 18-70
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Distant metastasis Absent
Item
no evidence of distant metastasis
boolean
C1269798 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Prior Therapy Absent
Item
no previous therapy
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Hematologic function
Item
normal hematologic function
boolean
C0221130 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction greater than 50 percent
boolean
C0428772 (UMLS CUI [1])
Abnormality Absent Renal function | Abnormality Absent Liver function
Item
no abnormality of renal or liver function
boolean
C1704258 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0232804 (UMLS CUI [1,3])
C1704258 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0232741 (UMLS CUI [2,3])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Constitution allergic | Allergic Reaction Possible Investigational New Drugs
Item
with allergic constitution or possible allergic reflection to drugs to be used in this study
boolean
C0683521 (UMLS CUI [1,1])
C0700624 (UMLS CUI [1,2])
C1527304 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
C0013230 (UMLS CUI [2,3])
Comorbidity Uncontrolled | Mental disorder Uncontrolled
Item
any concurrent uncontrolled medical or psychiatric disorder
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0004936 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
Heart Diseases Severe | Congestive heart failure | Angina, Unstable | Cardiac Arrhythmia Uncontrolled | Myocardial Infarction | Uncontrolled hypertension | Heart valve disease
Item
history of severe heart diseases, including congestive heart failure, unstable angina, uncontrolled arrhythmia, myocardial infarction, uncontrolled high blood pressure, or heart valve disease.
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0018802 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0003811 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
C0027051 (UMLS CUI [5])
C1868885 (UMLS CUI [6])
C0018824 (UMLS CUI [7])
Bleeding tendency
Item
history of bleeding diathesis
boolean
C1458140 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
being pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [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