ID

26983

Descripción

Positron Emission Mammography (PEM) Flex Solo II Positron Emission Tomography (PET) Scanner and Stereo Navigator Biopsy Accessory for the Diagnosis of Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00981812

Link

https://clinicaltrials.gov/show/NCT00981812

Palabras clave

  1. 29.10.17 29.10.17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

29. Oktober 2017

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Breast Cancer NCT00981812

Eligibility Breast Cancer NCT00981812

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
subject is 25-100 years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
subjects has at least one breast imaging finding on mammography and/or ultrasound which is assessed as highly suggestive of malignancy and recommended to biopsy
Descripción

Female Mammography Quantity Suggestive of Malignant Neoplasm | Mammary Ultrasonography Quantity Suggestive of Malignant Neoplasm | Recommendation Biopsy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0848600
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0332299
UMLS CUI [1,4]
C0006826
UMLS CUI [2,1]
C0080264
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0332299
UMLS CUI [2,4]
C0006826
UMLS CUI [3,1]
C0034866
UMLS CUI [3,2]
C0005558
subject is able to provide informed consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject is pregnant
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
subject is actively lactating or discontinued breastfeeding less than 2 months ago
Descripción

Breast Feeding | Breast Feeding Discontinued Recently

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006147
UMLS CUI [2,1]
C0006147
UMLS CUI [2,2]
C1444662
UMLS CUI [2,3]
C0332185
subject has breast implants
Descripción

Breast implants

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0179412
subject is scheduled for sentinel node procedure using radioactive tc-99m within 24 hours of the pem study
Descripción

Sentinel Lymph Node Biopsy Technetium 99m Scheduled | Positron Emission Mammography

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0796693
UMLS CUI [1,2]
C0303611
UMLS CUI [1,3]
C0205539
UMLS CUI [2]
C3897879
subject has contraindications for core biopsy and other invasive procedures
Descripción

Medical contraindication Core needle biopsy | Medical contraindication Invasive procedure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1318309
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C4048276
subject has type i diabetes mellitus or poorly controlled type ii diabetes mellitus
Descripción

Diabetes Mellitus, Insulin-Dependent | Type II diabetes mellitus uncontrolled

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C2733146
subject has had surgery or radiation therapy on the study breast or has had chemotherapy within the past 12 months
Descripción

Therapeutic radiology procedure Breast Involved | Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0006141
UMLS CUI [1,3]
C1314939
UMLS CUI [2]
C0392920
subject has not fasted for 4-6 hours prior to the procedure and/or have a fasting blood glucose level greater than 140 mg/dl on day of pem imaging
Descripción

Fasting Lacking | Fasting blood glucose measurement | Positron Emission Mammography

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0015663
UMLS CUI [1,2]
C0332268
UMLS CUI [2]
C0428568
UMLS CUI [3]
C3897879

Similar models

Eligibility Breast Cancer NCT00981812

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Age
Item
subject is 25-100 years of age
boolean
C0001779 (UMLS CUI [1])
Female Mammography Quantity Suggestive of Malignant Neoplasm | Mammary Ultrasonography Quantity Suggestive of Malignant Neoplasm | Recommendation Biopsy
Item
subjects has at least one breast imaging finding on mammography and/or ultrasound which is assessed as highly suggestive of malignancy and recommended to biopsy
boolean
C0848600 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0332299 (UMLS CUI [1,3])
C0006826 (UMLS CUI [1,4])
C0080264 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0332299 (UMLS CUI [2,3])
C0006826 (UMLS CUI [2,4])
C0034866 (UMLS CUI [3,1])
C0005558 (UMLS CUI [3,2])
Informed Consent
Item
subject is able to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
subject is pregnant
boolean
C0032961 (UMLS CUI [1])
Breast Feeding | Breast Feeding Discontinued Recently
Item
subject is actively lactating or discontinued breastfeeding less than 2 months ago
boolean
C0006147 (UMLS CUI [1])
C0006147 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C0332185 (UMLS CUI [2,3])
Breast implants
Item
subject has breast implants
boolean
C0179412 (UMLS CUI [1])
Sentinel Lymph Node Biopsy Technetium 99m Scheduled | Positron Emission Mammography
Item
subject is scheduled for sentinel node procedure using radioactive tc-99m within 24 hours of the pem study
boolean
C0796693 (UMLS CUI [1,1])
C0303611 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C3897879 (UMLS CUI [2])
Medical contraindication Core needle biopsy | Medical contraindication Invasive procedure
Item
subject has contraindications for core biopsy and other invasive procedures
boolean
C1301624 (UMLS CUI [1,1])
C1318309 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C4048276 (UMLS CUI [2,2])
Diabetes Mellitus, Insulin-Dependent | Type II diabetes mellitus uncontrolled
Item
subject has type i diabetes mellitus or poorly controlled type ii diabetes mellitus
boolean
C0011854 (UMLS CUI [1])
C2733146 (UMLS CUI [2])
Therapeutic radiology procedure Breast Involved | Chemotherapy
Item
subject has had surgery or radiation therapy on the study breast or has had chemotherapy within the past 12 months
boolean
C1522449 (UMLS CUI [1,1])
C0006141 (UMLS CUI [1,2])
C1314939 (UMLS CUI [1,3])
C0392920 (UMLS CUI [2])
Fasting Lacking | Fasting blood glucose measurement | Positron Emission Mammography
Item
subject has not fasted for 4-6 hours prior to the procedure and/or have a fasting blood glucose level greater than 140 mg/dl on day of pem imaging
boolean
C0015663 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0428568 (UMLS CUI [2])
C3897879 (UMLS CUI [3])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

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