ID

19553

Beschrijving

Randomized Phase II Trial Induction Therapy for Early Stage Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00209092

Link

https://clinicaltrials.gov/show/NCT00209092

Trefwoorden

  1. 10-01-17 10-01-17 -
Geüploaded op

10 januari 2017

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 Cancer NCT00209092

Eligibility Breast Cancer NCT00209092

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically or cytologically confirmed breast carcinoma.
Beschrijving

Breast Carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0678222
early stage breast cancer (stage 1, 2, 3).
Beschrijving

Early-Stage Breast Carcinoma TNM clinical staging

Datatype

boolean

Alias
UMLS CUI [1,1]
C2986665
UMLS CUI [1,2]
C3258246
no evidence of disease outside the breast or chest wall, except ipsilateral axillary lymph nodes.
Beschrijving

Disease Breast outside Evidence | Disease chest wall outside Evidence | Disease Axillary lymph nodes Ipsilateral

Datatype

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0006141
UMLS CUI [1,3]
C0205101
UMLS CUI [1,4]
C3887511
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C1279035
UMLS CUI [2,3]
C0205101
UMLS CUI [2,4]
C3887511
UMLS CUI [3,1]
C0012634
UMLS CUI [3,2]
C0729594
UMLS CUI [3,3]
C0441989
18 years of age or older.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
Beschrijving

Eligibility Determination Research Personnel

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013893
UMLS CUI [1,2]
C0035173
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior chemotherapy, hormonal therapy, biologic therapy or radiation therapy for breast cancer.
Beschrijving

Chemotherapy Breast Carcinoma | Hormone Therapy Breast Carcinoma | Biological treatment Breast Carcinoma | Therapeutic radiology procedure Breast Carcinoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0678222
UMLS CUI [2,1]
C0279025
UMLS CUI [2,2]
C0678222
UMLS CUI [3,1]
C1531518
UMLS CUI [3,2]
C0678222
UMLS CUI [4,1]
C1522449
UMLS CUI [4,2]
C0678222
major surgery within 28 days of study entry.
Beschrijving

major surgery

Datatype

boolean

Alias
UMLS CUI [1]
C0679637
evidence of central nervous system (cns) metastases.
Beschrijving

CNS metastases Evidence of

Datatype

boolean

Alias
UMLS CUI [1,1]
C0686377
UMLS CUI [1,2]
C0332120
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
Beschrijving

Eligibility Determination Research Personnel

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013893
UMLS CUI [1,2]
C0035173

Similar models

Eligibility Breast Cancer NCT00209092

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma
Item
histologically or cytologically confirmed breast carcinoma.
boolean
C0678222 (UMLS CUI [1])
Early-Stage Breast Carcinoma TNM clinical staging
Item
early stage breast cancer (stage 1, 2, 3).
boolean
C2986665 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
Disease Breast outside Evidence | Disease chest wall outside Evidence | Disease Axillary lymph nodes Ipsilateral
Item
no evidence of disease outside the breast or chest wall, except ipsilateral axillary lymph nodes.
boolean
C0012634 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
C0205101 (UMLS CUI [1,3])
C3887511 (UMLS CUI [1,4])
C0012634 (UMLS CUI [2,1])
C1279035 (UMLS CUI [2,2])
C0205101 (UMLS CUI [2,3])
C3887511 (UMLS CUI [2,4])
C0012634 (UMLS CUI [3,1])
C0729594 (UMLS CUI [3,2])
C0441989 (UMLS CUI [3,3])
Age
Item
18 years of age or older.
boolean
C0001779 (UMLS CUI [1])
Eligibility Determination Research Personnel
Item
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
boolean
C0013893 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Chemotherapy Breast Carcinoma | Hormone Therapy Breast Carcinoma | Biological treatment Breast Carcinoma | Therapeutic radiology procedure Breast Carcinoma
Item
prior chemotherapy, hormonal therapy, biologic therapy or radiation therapy for breast cancer.
boolean
C0392920 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0279025 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C1531518 (UMLS CUI [3,1])
C0678222 (UMLS CUI [3,2])
C1522449 (UMLS CUI [4,1])
C0678222 (UMLS CUI [4,2])
major surgery
Item
major surgery within 28 days of study entry.
boolean
C0679637 (UMLS CUI [1])
CNS metastases Evidence of
Item
evidence of central nervous system (cns) metastases.
boolean
C0686377 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
Eligibility Determination Research Personnel
Item
final eligibility for a clinical trial is determined by the health professionals conducting the trial.
boolean
C0013893 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])

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