ID

38103

Beschreibung

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

Stichworte

  1. 17.09.19 17.09.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

17. September 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01737970

Eligibility Breast Cancer NCT01737970

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
participant is willing and able to give informed consent for participation in the study.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
has an established diagnosis of locally advanced breast cancer.
Beschreibung

Locally advanced breast cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C3495949
aged 18 years or above.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
history of previous breast cancer does not exclude from study.
Beschreibung

Breast Carcinoma Previous

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205156
having neoadjuvant chemotherapy delivered in oxford cancer centre.
Beschreibung

Neoadjuvant Chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C3665472
good general health
Beschreibung

General health good

Datentyp

boolean

Alias
UMLS CUI [1]
C1277245
blood tests to check suitability for the diagnostic core biopsy
Beschreibung

Hematologic Tests | Check Appropriateness Core biopsy

Datentyp

boolean

Alias
UMLS CUI [1]
C0018941
UMLS CUI [2,1]
C1283174
UMLS CUI [2,2]
C0814634
UMLS CUI [2,3]
C1318309
having a localisation coil as part of routine medical care.
Beschreibung

Localization Coil | Part Medical care

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0475264
UMLS CUI [1,2]
C1705946
UMLS CUI [2,1]
C0449719
UMLS CUI [2,2]
C0496675
patients who are recruited into other studies can be included if there is no conflict of interest and the patient is in agreement.
Beschreibung

Study Subject Participation Status | Conflict of Interest Absent

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0079152
UMLS CUI [2,2]
C0332197
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
any co-morbidity that is likely to prevent regular attendance.
Beschreibung

Comorbidity Preventing Attendance

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C1292733
UMLS CUI [1,3]
C2827364
is <18 years of age or over 70 years.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
has a movement disorder as the patient is required to lie very still for a few minutes during the scan.
Beschreibung

Movement Disorder

Datentyp

boolean

Alias
UMLS CUI [1]
C0026650

Ähnliche Modelle

Eligibility Breast Cancer NCT01737970

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
Neoadjuvant Chemotherapy
Item
having neoadjuvant chemotherapy delivered in oxford cancer centre.
boolean
C0600558 (UMLS CUI [1,1])
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])
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])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])

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