ID

12430

Beschreibung

Breast VCEUS to Evaluate Early Response to Neoadjuvant Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT01817374

Link

https://clinicaltrials.gov/show/NCT01817374

Stichworte

  1. 17.11.15 17.11.15 -
  2. 17.11.15 17.11.15 - Julian Varghese
Hochgeladen am

17. November 2015

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01817374

Eligibility Breast Cancer NCT01817374

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. adult patients (age 19 years or older).
Beschreibung

age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
2. patients with newly diagnosed and untreated stage ii and iii breast cancer scheduled to undergo neoadjuvant chemotherapy.
Beschreibung

Patients with newly diagnosed and untreated stage ii and iii breast cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C0006142
3. patients with signed informed consent.
Beschreibung

Informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. any history of prior radiation or chemotherapy for breast cancer.
Beschreibung

Any history of prior radiation or chemotherapy for breast cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C1300985
2. patients who only have non-measurable disease.
Beschreibung

Patients who only have non-measurable disease

Datentyp

boolean

Alias
UMLS CUI [1]
C3538912
3. patients who are medically unstable.
Beschreibung

Patients who are medically unstable

Datentyp

boolean

Alias
UMLS CUI [1]
C3841317
4. patients with other primary cancers requiring systemic treatment.
Beschreibung

Primary malignant neoplasm

Datentyp

boolean

Alias
UMLS CUI [1]
C1306459
5. patients with cardiac shunts.
Beschreibung

Cardiac shunt

Datentyp

boolean

Alias
UMLS CUI [1]
C0232180
6. patients with unstable cardiopulmonary conditions.
Beschreibung

Patients with unstable cardiopulmonary conditions

Datentyp

boolean

Alias
UMLS CUI [1]
C0238074
7. patients with known pulmonary hypertension.
Beschreibung

Pulmonary Hypertension

Datentyp

boolean

Alias
UMLS CUI [1]
C0020542
8. patients with known hypersensitivity to any component of definity (r) microbubble contrast.
Beschreibung

Patients with known hypersensitivity

Datentyp

boolean

Alias
UMLS CUI [1]
C0020517
9. patients who are pregnant, breast-feeding or are planning to become pregnant during the study duration.
Beschreibung

pregnant and breast feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0006147
UMLS CUI [2]
C0032961

Ähnliche Modelle

Eligibility Breast Cancer NCT01817374

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
1. adult patients (age 19 years or older).
boolean
C0001779 (UMLS CUI [1])
Patients with newly diagnosed and untreated stage ii and iii breast cancer
Item
2. patients with newly diagnosed and untreated stage ii and iii breast cancer scheduled to undergo neoadjuvant chemotherapy.
boolean
C0006142 (UMLS CUI [1])
Informed consent
Item
3. patients with signed informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Any history of prior radiation or chemotherapy for breast cancer
Item
1. any history of prior radiation or chemotherapy for breast cancer.
boolean
C1300985 (UMLS CUI [1])
Patients who only have non-measurable disease
Item
2. patients who only have non-measurable disease.
boolean
C3538912 (UMLS CUI [1])
Patients who are medically unstable
Item
3. patients who are medically unstable.
boolean
C3841317 (UMLS CUI [1])
Primary malignant neoplasm
Item
4. patients with other primary cancers requiring systemic treatment.
boolean
C1306459 (UMLS CUI [1])
Cardiac shunt
Item
5. patients with cardiac shunts.
boolean
C0232180 (UMLS CUI [1])
Patients with unstable cardiopulmonary conditions
Item
6. patients with unstable cardiopulmonary conditions.
boolean
C0238074 (UMLS CUI [1])
Pulmonary Hypertension
Item
7. patients with known pulmonary hypertension.
boolean
C0020542 (UMLS CUI [1])
Patients with known hypersensitivity
Item
8. patients with known hypersensitivity to any component of definity (r) microbubble contrast.
boolean
C0020517 (UMLS CUI [1])
pregnant and breast feeding
Item
9. patients who are pregnant, breast-feeding or are planning to become pregnant during the study duration.
boolean
C0006147 (UMLS CUI [1])
C0032961 (UMLS CUI [2])

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