Informatie:
Fout:
ID
19577
Beschrijving
A Trial of Paclitaxel and Bevacizumab vs. Gemcitabine, Paclitaxel, and Bevacizumab in Advanced Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00320541
Link
https://clinicaltrials.gov/show/NCT00320541
Trefwoorden
Versies (1)
- 11-01-17 11-01-17 -
Geüploaded op
11 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 NCT00320541
Eligibility Breast Cancer NCT00320541
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00320541
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Female Breast Carcinoma | Neoplasm Metastasis Breast | Neoplasm Metastasis Organs
Item
females diagnosed with breast cancer and the cancer has spread to distant areas of the breast or organs.
boolean
C0007104 (UMLS CUI [1])
C0027627 (UMLS CUI [2,1])
C0006141 (UMLS CUI [2,2])
C0027627 (UMLS CUI [3,1])
C0178784 (UMLS CUI [3,2])
C0027627 (UMLS CUI [2,1])
C0006141 (UMLS CUI [2,2])
C0027627 (UMLS CUI [3,1])
C0178784 (UMLS CUI [3,2])
Measurable Disease Parameters Medical
Item
must be able to measure the disease by specific medical parameters
boolean
C1513041 (UMLS CUI [1,1])
C0449381 (UMLS CUI [1,2])
C0205476 (UMLS CUI [1,3])
C0449381 (UMLS CUI [1,2])
C0205476 (UMLS CUI [1,3])
Therapeutic procedure Early-Stage Breast Carcinoma
Item
may have received breast cancer treatment in the early stage of the disease
boolean
C0087111 (UMLS CUI [1,1])
C2986665 (UMLS CUI [1,2])
C2986665 (UMLS CUI [1,2])
Strenuous Exercise Restricted | Light Work Perform Able
Item
may be restricted in physically strenuous activity but able to carry out light work.
boolean
C1514989 (UMLS CUI [1,1])
C0443288 (UMLS CUI [1,2])
C2987220 (UMLS CUI [2,1])
C0884358 (UMLS CUI [2,2])
C0085732 (UMLS CUI [2,3])
C0443288 (UMLS CUI [1,2])
C2987220 (UMLS CUI [2,1])
C0884358 (UMLS CUI [2,2])
C0085732 (UMLS CUI [2,3])
Organ function Blood test result
Item
must have adequate organ function as seen in blood test results.
boolean
C0678852 (UMLS CUI [1,1])
C0849535 (UMLS CUI [1,2])
C0849535 (UMLS CUI [1,2])
Exclusion Criteria
Item
exclusion
boolean
C0680251 (UMLS CUI [1])
criteria
Item
criteria:
boolean
C0243161 (UMLS CUI [1])
Metastatic malignant neoplasm to brain
Item
cancer that has spread to the brain.
boolean
C0220650 (UMLS CUI [1])
HEART PROBLEM Unstable
Item
unstable heart problems
boolean
C0795691 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,2])
Hypertensive disease Unstable
Item
unstable high blood pressure.
boolean
C0020538 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,2])
Neoplasm Metastasis | Therapeutic procedure Breast Carcinoma
Item
breast cancer treatment after the disease has considered to spread to other areas or organs.
boolean
C0027627 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
Protocol Compliance Unable
Item
unable to agree with the requirements of the study
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])