Informationen:
Fehler:
ID
26306
Beschreibung
Determination of Predictive Value of Echography Doppler Abnormalities; ODM derived from: https://clinicaltrials.gov/show/NCT00714909
Link
https://clinicaltrials.gov/show/NCT00714909
Stichworte
Versionen (1)
- 16.10.17 16.10.17 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
16. Oktober 2017
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Breast Cancer NCT00714909
Eligibility Breast Cancer NCT00714909
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT00714909
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Gender | Age
Item
women over 18
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
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])
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])
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])
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])
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])
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])
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])
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])
C0076611 (UMLS CUI [2])
C0337428 (UMLS CUI [3])
Creatinine measurement, serum
Item
creatinin > 175mole/l
boolean
C0201976 (UMLS CUI [1])