ID

33440

Description

Quality of Life in Metastatic Breast Cancer (MBC) Patients in Second Line Monochemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT02403869

Link

https://clinicaltrials.gov/show/NCT02403869

Keywords

  1. 12/9/18 12/9/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

December 9, 2018

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Breast Neoplasms NCT02403869

Eligibility Breast Neoplasms NCT02403869

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who give their written informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
patients with metastatic breast cancer who start treatment with second-line monochemotherapy.
Description

Secondary malignant neoplasm of female breast | Second line Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0346993
UMLS CUI [2,1]
C1710038
UMLS CUI [2,2]
C0392920
patients of both sexes, at least 18 years of age and of any race.
Description

Age | Racial group Any

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0034510
UMLS CUI [2,2]
C1552551
patients with life expectancy longer than or equal to 12 weeks.
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
patients with histological or cytological diagnosis of her-2/neu negative breast adenocarcinoma.
Description

Breast adenocarcinoma HER2/Neu Negative

Data type

boolean

Alias
UMLS CUI [1,1]
C0858252
UMLS CUI [1,2]
C2348908
patients with ability enough to understand the questionnaires.
Description

Comprehension Questionnaires

Data type

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C0034394
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or lactating women.
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients who are participating or have participated in a clinical trial in the last two months.
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
patients who refuse to participate in the study.
Description

Refusal to Participate Clinical Trial

Data type

boolean

Alias
UMLS CUI [1,1]
C1136454
UMLS CUI [1,2]
C0008976

Similar models

Eligibility Breast Neoplasms NCT02403869

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
patients who give their written informed consent.
boolean
C0021430 (UMLS CUI [1])
Secondary malignant neoplasm of female breast | Second line Chemotherapy
Item
patients with metastatic breast cancer who start treatment with second-line monochemotherapy.
boolean
C0346993 (UMLS CUI [1])
C1710038 (UMLS CUI [2,1])
C0392920 (UMLS CUI [2,2])
Age | Racial group Any
Item
patients of both sexes, at least 18 years of age and of any race.
boolean
C0001779 (UMLS CUI [1])
C0034510 (UMLS CUI [2,1])
C1552551 (UMLS CUI [2,2])
Life Expectancy
Item
patients with life expectancy longer than or equal to 12 weeks.
boolean
C0023671 (UMLS CUI [1])
Breast adenocarcinoma HER2/Neu Negative
Item
patients with histological or cytological diagnosis of her-2/neu negative breast adenocarcinoma.
boolean
C0858252 (UMLS CUI [1,1])
C2348908 (UMLS CUI [1,2])
Comprehension Questionnaires
Item
patients with ability enough to understand the questionnaires.
boolean
C0162340 (UMLS CUI [1,1])
C0034394 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
pregnant or lactating women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
patients who are participating or have participated in a clinical trial in the last two months.
boolean
C2348568 (UMLS CUI [1])
Refusal to Participate Clinical Trial
Item
patients who refuse to participate in the study.
boolean
C1136454 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

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