ID

26306

Description

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

Lien

https://clinicaltrials.gov/show/NCT00714909

Mots-clés

Versions (1)
  1. 16/10/2017 16/10/2017 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

16 octobre 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00714909

Anglais

Eligibility Breast Cancer NCT00714909

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
women over 18
Description

Gender | Age

Type de données

boolean

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

Breast Carcinoma

Type de données

boolean

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

Breast Carcinoma Localized | Neoplasm Metastasis Absent

Type de données

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
Description

Chemotherapy, Adjuvant | Chemotherapy Neoadjuvant

Type de données

boolean

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

Insertion Central venous catheter Port | Chemotherapy

Type de données

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
Description

Central venous catheter Duration

Type de données

boolean

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

Informed Consent

Type de données

boolean

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

Follow-up

Type de données

boolean

Alias
UMLS CUI [1]
C3274571
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
ongoing anticoagulant therapy
Description

Anticoagulation Therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0003281
previous central catheter
Description

Central venous catheter Previous

Type de données

boolean

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

Catheter, Femoral

Type de données

boolean

Alias
UMLS CUI [1]
C1879462
double lumen catheter
Description

Double lumen catheter

Type de données

boolean

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

Central venous catheter Without Port

Type de données

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
Description

Platelet Count measurement | thymoquinone | Fibrinogen level

Type de données

boolean

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

Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
Retour au début de la page

Similar models

Eligibility Breast Cancer NCT00714909

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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])
Retour au début de la page 

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