ID

34167

Description

Cardiotoxicity of Adjuvant Trastuzumab; ODM derived from: https://clinicaltrials.gov/show/NCT00858039

Lien

https://clinicaltrials.gov/show/NCT00858039

Mots-clés

  1. 14/01/2019 14/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

14 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Breast Neoplasms NCT00858039

Eligibility Breast Neoplasms NCT00858039

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female 18 years or older
Description

ID.1

Type de données

boolean

histologically confirmed, completely excised invasive breast cancer with her-2 overexpression
Description

ID.2

Type de données

boolean

primary surgery less than twelve weeks prior to registration
Description

ID.3

Type de données

boolean

lvef>50% as assessed by transthoracic echocardiogram or gated heart pool scan
Description

ID.4

Type de données

boolean

eastern cooperative oncology group performance status 0-2
Description

ID.5

Type de données

boolean

adjuvant systemic treatment plan comprises at least three cycles of anthracycline chemotherapy and 52 weeks of trastuzumab
Description

ID.6

Type de données

boolean

before patient registration, informed consent must be given according to local regulations.
Description

ID.7

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Description

ID.8

Type de données

boolean

distant metastases from breast cancer
Description

ID.9

Type de données

boolean

any systemic chemotherapy prior to study entry
Description

ID.10

Type de données

boolean

Similar models

Eligibility Breast Neoplasms NCT00858039

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
female 18 years or older
boolean
ID.2
Item
histologically confirmed, completely excised invasive breast cancer with her-2 overexpression
boolean
ID.3
Item
primary surgery less than twelve weeks prior to registration
boolean
ID.4
Item
lvef>50% as assessed by transthoracic echocardiogram or gated heart pool scan
boolean
ID.5
Item
eastern cooperative oncology group performance status 0-2
boolean
ID.6
Item
adjuvant systemic treatment plan comprises at least three cycles of anthracycline chemotherapy and 52 weeks of trastuzumab
boolean
ID.7
Item
before patient registration, informed consent must be given according to local regulations.
boolean
Item Group
C0680251 (UMLS CUI)
ID.8
Item
pregnancy
boolean
ID.9
Item
distant metastases from breast cancer
boolean
ID.10
Item
any systemic chemotherapy prior to study entry
boolean

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