ID

26306

Descripción

Determination of Predictive Value of Echography Doppler Abnormalities; ODM derived from: https://clinicaltrials.gov/show/NCT00714909

Link

https://clinicaltrials.gov/show/NCT00714909

Palabras clave

  1. 16/10/17 16/10/17 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

16 de octubre de 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 NCT00714909

Eligibility Breast Cancer NCT00714909

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
women over 18
Descripción

Gender | Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
histologically proven breast cancer
Descripción

Breast Carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0678222
localized breast cancer without metastasis
Descripción

Breast Carcinoma Localized | Neoplasm Metastasis Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0392752
UMLS CUI [2,1]
C0027627
UMLS CUI [2,2]
C0332197
adjuvant or neo adjuvant chemotherapy
Descripción

Chemotherapy, Adjuvant | Chemotherapy Neoadjuvant

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0085533
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0600558
insertion of central catheter with port for chemotherapy
Descripción

Insertion Central venous catheter Port | Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0021107
UMLS CUI [1,2]
C1145640
UMLS CUI [1,3]
C1706409
UMLS CUI [2]
C0392920
central catheter for more than three months
Descripción

Central venous catheter Duration

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1145640
UMLS CUI [1,2]
C0449238
inform consent
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
follow up for three months
Descripción

Follow-up

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3274571
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
ongoing anticoagulant therapy
Descripción

Anticoagulation Therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003281
previous central catheter
Descripción

Central venous catheter Previous

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1145640
UMLS CUI [1,2]
C0205156
femoral catheter
Descripción

Catheter, Femoral

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1879462
double lumen catheter
Descripción

Double lumen catheter

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0441131
central catheter without port
Descripción

Central venous catheter Without Port

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1145640
UMLS CUI [1,2]
C0332288
UMLS CUI [1,3]
C1706409
platelets < 80g/l, tq < 50%, fibrinogen < 1 g/l
Descripción

Platelet Count measurement | thymoquinone | Fibrinogen level

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032181
UMLS CUI [2]
C0076611
UMLS CUI [3]
C0337428
creatinin > 175mole/l
Descripción

Creatinine measurement, serum

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201976

Similar models

Eligibility Breast Cancer NCT00714909

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
women over 18
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Breast Carcinoma
Item
histologically proven breast cancer
boolean
C0678222 (UMLS CUI [1])
Breast Carcinoma Localized | Neoplasm Metastasis Absent
Item
localized breast cancer without metastasis
boolean
C0678222 (UMLS CUI [1,1])
C0392752 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Chemotherapy, Adjuvant | Chemotherapy Neoadjuvant
Item
adjuvant or neo adjuvant chemotherapy
boolean
C0085533 (UMLS CUI [1])
C0392920 (UMLS CUI [2,1])
C0600558 (UMLS CUI [2,2])
Insertion Central venous catheter Port | Chemotherapy
Item
insertion of central catheter with port for chemotherapy
boolean
C0021107 (UMLS CUI [1,1])
C1145640 (UMLS CUI [1,2])
C1706409 (UMLS CUI [1,3])
C0392920 (UMLS CUI [2])
Central venous catheter Duration
Item
central catheter for more than three months
boolean
C1145640 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Informed Consent
Item
inform consent
boolean
C0021430 (UMLS CUI [1])
Follow-up
Item
follow up for three months
boolean
C3274571 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Anticoagulation Therapy
Item
ongoing anticoagulant therapy
boolean
C0003281 (UMLS CUI [1])
Central venous catheter Previous
Item
previous central catheter
boolean
C1145640 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Catheter, Femoral
Item
femoral catheter
boolean
C1879462 (UMLS CUI [1])
Double lumen catheter
Item
double lumen catheter
boolean
C0441131 (UMLS CUI [1])
Central venous catheter Without Port
Item
central catheter without port
boolean
C1145640 (UMLS CUI [1,1])
C0332288 (UMLS CUI [1,2])
C1706409 (UMLS CUI [1,3])
Platelet Count measurement | thymoquinone | Fibrinogen level
Item
platelets < 80g/l, tq < 50%, fibrinogen < 1 g/l
boolean
C0032181 (UMLS CUI [1])
C0076611 (UMLS CUI [2])
C0337428 (UMLS CUI [3])
Creatinine measurement, serum
Item
creatinin > 175mole/l
boolean
C0201976 (UMLS CUI [1])

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