Informatie:
Fout:
ID
38103
Beschrijving
A Study to Correlate Ultrasound Elastography With Histopathology to Monitor the Response of Locally Advanced Breast Cancer to Neoadjuvant Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT01737970
Link
https://clinicaltrials.gov/show/NCT01737970
Trefwoorden
Versies (1)
- 17-09-19 17-09-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
17 september 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 Cancer NCT01737970
Eligibility Breast Cancer NCT01737970
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01737970
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Informed Consent
Item
participant is willing and able to give informed consent for participation in the study.
boolean
C0021430 (UMLS CUI [1])
Locally advanced breast cancer
Item
has an established diagnosis of locally advanced breast cancer.
boolean
C3495949 (UMLS CUI [1])
Age
Item
aged 18 years or above.
boolean
C0001779 (UMLS CUI [1])
Breast Carcinoma Previous
Item
history of previous breast cancer does not exclude from study.
boolean
C0678222 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,2])
Neoadjuvant Chemotherapy
Item
having neoadjuvant chemotherapy delivered in oxford cancer centre.
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (UMLS CUI [1,2])
C3665472 (UMLS CUI [1,2])
General health good
Item
good general health
boolean
C1277245 (UMLS CUI [1])
Hematologic Tests | Check Appropriateness Core biopsy
Item
blood tests to check suitability for the diagnostic core biopsy
boolean
C0018941 (UMLS CUI [1])
C1283174 (UMLS CUI [2,1])
C0814634 (UMLS CUI [2,2])
C1318309 (UMLS CUI [2,3])
C1283174 (UMLS CUI [2,1])
C0814634 (UMLS CUI [2,2])
C1318309 (UMLS CUI [2,3])
Localization Coil | Part Medical care
Item
having a localisation coil as part of routine medical care.
boolean
C0475264 (UMLS CUI [1,1])
C1705946 (UMLS CUI [1,2])
C0449719 (UMLS CUI [2,1])
C0496675 (UMLS CUI [2,2])
C1705946 (UMLS CUI [1,2])
C0449719 (UMLS CUI [2,1])
C0496675 (UMLS CUI [2,2])
Study Subject Participation Status | Conflict of Interest Absent
Item
patients who are recruited into other studies can be included if there is no conflict of interest and the patient is in agreement.
boolean
C2348568 (UMLS CUI [1])
C0079152 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0079152 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Comorbidity Preventing Attendance
Item
any co-morbidity that is likely to prevent regular attendance.
boolean
C0009488 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C2827364 (UMLS CUI [1,3])
C1292733 (UMLS CUI [1,2])
C2827364 (UMLS CUI [1,3])
Age
Item
is <18 years of age or over 70 years.
boolean
C0001779 (UMLS CUI [1])
Movement Disorder
Item
has a movement disorder as the patient is required to lie very still for a few minutes during the scan.
boolean
C0026650 (UMLS CUI [1])