ID

37941

Beschreibung

Comparing the Efficacy and Tolerability of Fulvestrant 500 mg Versus 250 mg in Advanced Breast Cancer Women; ODM derived from: https://clinicaltrials.gov/show/NCT01300351

Link

https://clinicaltrials.gov/show/NCT01300351

Stichworte

Versionen (1)
  1. 01.09.19 01.09.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

1. 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.

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 Cancer NCT01300351

Englisch

Eligibility Breast Cancer NCT01300351

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
postmenopausal women defined as a woman who has stopped having menstrual periods
Beschreibung

Postmenopausal state

Datentyp

boolean

Alias
UMLS CUI [1]
C0232970
breast cancer has continued to grow after having received treatment with an anti-estrogen hormonal treatment such as tamoxifen or an aromatase inhibitor
Beschreibung

Breast Carcinoma | Disease Progression | Status post Antioestrogen therapy | Tamoxifen | Aromatase Inhibitors

Datentyp

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2]
C0242656
UMLS CUI [3,1]
C0231290
UMLS CUI [3,2]
C0854638
UMLS CUI [4]
C0039286
UMLS CUI [5]
C0593802
requiring hormonal treatment
Beschreibung

Requirement Hormone Therapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1514873
UMLS CUI [1,2]
C0279025
oestrogen-receptor positive tumour
Beschreibung

Estrogen receptor positive tumor

Datentyp

boolean

Alias
UMLS CUI [1]
C1562312
written informed consent to participate in the trial
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
treatment with an investigational or non-approved drug within one month
Beschreibung

Investigational New Drugs | Drugs, Non-Prescription

Datentyp

boolean

Alias
UMLS CUI [1]
C0013230
UMLS CUI [2]
C0013231
an existing serious disease, illness, or condition that will prevent participation or compliance with study procedures
Beschreibung

Illness Serious Study Subject Participation Status Excluded | Condition Serious Study Subject Participation Status Excluded | Illness Serious Preventing Protocol Compliance | Condition Serious Preventing Protocol Compliance

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C2348568
UMLS CUI [1,4]
C0332196
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0205404
UMLS CUI [2,3]
C2348568
UMLS CUI [2,4]
C0332196
UMLS CUI [3,1]
C0221423
UMLS CUI [3,2]
C0205404
UMLS CUI [3,3]
C1292733
UMLS CUI [3,4]
C0525058
UMLS CUI [4,1]
C0348080
UMLS CUI [4,2]
C0205404
UMLS CUI [4,3]
C1292733
UMLS CUI [4,4]
C0525058
a history of allergies to any active or inactive ingredients of fulvestrant (i.e. castor oil)
Beschreibung

Hypersensitivity Fulvestrant Ingredient | Castor oil allergy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0935916
UMLS CUI [1,3]
C1550600
UMLS CUI [2]
C0571232
treatment with more than one regimen of chemotherapy for advanced breast cancer
Beschreibung

Chemotherapy Regimen Quantity Advanced breast cancer

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C3495917
treatment with more than one regimen of hormonal treatment for advanced breast cancer
Beschreibung

Hormone Therapy Quantity Advanced breast cancer

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C3495917
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Breast Cancer NCT01300351

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Postmenopausal state
Item
postmenopausal women defined as a woman who has stopped having menstrual periods
boolean
C0232970 (UMLS CUI [1])
Breast Carcinoma | Disease Progression | Status post Antioestrogen therapy | Tamoxifen | Aromatase Inhibitors
Item
breast cancer has continued to grow after having received treatment with an anti-estrogen hormonal treatment such as tamoxifen or an aromatase inhibitor
boolean
C0678222 (UMLS CUI [1])
C0242656 (UMLS CUI [2])
C0231290 (UMLS CUI [3,1])
C0854638 (UMLS CUI [3,2])
C0039286 (UMLS CUI [4])
C0593802 (UMLS CUI [5])
Requirement Hormone Therapy
Item
requiring hormonal treatment
boolean
C1514873 (UMLS CUI [1,1])
C0279025 (UMLS CUI [1,2])
Estrogen receptor positive tumor
Item
oestrogen-receptor positive tumour
boolean
C1562312 (UMLS CUI [1])
Informed Consent
Item
written informed consent to participate in the trial
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Investigational New Drugs | Drugs, Non-Prescription
Item
treatment with an investigational or non-approved drug within one month
boolean
C0013230 (UMLS CUI [1])
C0013231 (UMLS CUI [2])
Illness Serious Study Subject Participation Status Excluded | Condition Serious Study Subject Participation Status Excluded | Illness Serious Preventing Protocol Compliance | Condition Serious Preventing Protocol Compliance
Item
an existing serious disease, illness, or condition that will prevent participation or compliance with study procedures
boolean
C0221423 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C0332196 (UMLS CUI [1,4])
C0348080 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C2348568 (UMLS CUI [2,3])
C0332196 (UMLS CUI [2,4])
C0221423 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C1292733 (UMLS CUI [3,3])
C0525058 (UMLS CUI [3,4])
C0348080 (UMLS CUI [4,1])
C0205404 (UMLS CUI [4,2])
C1292733 (UMLS CUI [4,3])
C0525058 (UMLS CUI [4,4])
Hypersensitivity Fulvestrant Ingredient | Castor oil allergy
Item
a history of allergies to any active or inactive ingredients of fulvestrant (i.e. castor oil)
boolean
C0020517 (UMLS CUI [1,1])
C0935916 (UMLS CUI [1,2])
C1550600 (UMLS CUI [1,3])
C0571232 (UMLS CUI [2])
Chemotherapy Regimen Quantity Advanced breast cancer
Item
treatment with more than one regimen of chemotherapy for advanced breast cancer
boolean
C0392920 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C3495917 (UMLS CUI [1,3])
Hormone Therapy Quantity Advanced breast cancer
Item
treatment with more than one regimen of hormonal treatment for advanced breast cancer
boolean
C0279025 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C3495917 (UMLS CUI [1,3])
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