ID

34167

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00858039

Trefwoorden

  1. 14-01-19 14-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

14 januari 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Breast Neoplasms NCT00858039

Eligibility Breast Neoplasms NCT00858039

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
female 18 years or older
Beschrijving

ID.1

Datatype

boolean

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

ID.2

Datatype

boolean

primary surgery less than twelve weeks prior to registration
Beschrijving

ID.3

Datatype

boolean

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

ID.4

Datatype

boolean

eastern cooperative oncology group performance status 0-2
Beschrijving

ID.5

Datatype

boolean

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

ID.6

Datatype

boolean

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

ID.7

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Beschrijving

ID.8

Datatype

boolean

distant metastases from breast cancer
Beschrijving

ID.9

Datatype

boolean

any systemic chemotherapy prior to study entry
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Breast Neoplasms NCT00858039

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial