Informationen:
Fehler:
ID
16327
Beschreibung
BREAST-10: Three-weekly Versus Weekly First-line Chemotherapy for Metastatic or Locally Advanced Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00540800
Link
https://clinicaltrials.gov/show/NCT00540800
Stichworte
Versionen (1)
- 11.07.16 11.07.16 -
Hochgeladen am
11. Juli 2016
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 NCT00540800
Eligibility Breast Cancer NCT00540800
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT00540800
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
diagnosis of breast cancer
Item
histological diagnosis of breast cancer
boolean
C0019638 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,2])
inoperable locally advanced or metastatic disease
Item
inoperable locally advanced or metastatic disease not yet treated with first-line chemotherapy
boolean
C3495949 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C0278488 (UMLS CUI [2])
C0205187 (UMLS CUI [1,2])
C0278488 (UMLS CUI [2])
Age
Item
age < 70 years
boolean
C0001779 (UMLS CUI [1])
ecog performance status
Item
ecog performance status < 2
boolean
C1520224 (UMLS CUI [1])
written informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
previous or concomitant malignant neoplasm
Item
previous or concomitant malignant neoplasm (excluding adequately treated baso or spinocellular skin carcinoma or carcinoma in situ of the cervix)
boolean
C0006826 (UMLS CUI [1])
docetaxel
Item
previous treatment with docetaxel
boolean
C0246415 (UMLS CUI [1])
symptomatic brain metastases
Item
symptomatic brain metastases
boolean
C0220650 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0231220 (UMLS CUI [1,2])
Neutrophil, platelets, haemoglobin
Item
neutrophil < 2000/mm3, platelets < 100,000/mm3, haemoglobin < 10 g/dl
boolean
C0200633 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0518015 (UMLS CUI [3])
C0032181 (UMLS CUI [2])
C0518015 (UMLS CUI [3])
creatinine
Item
creatinine > 1.25 x the upper normal limits
boolean
C0201976 (UMLS CUI [1])
transaminases
Item
got and/or gpt > 1.25 x the upper normal limits in absence of hepatic metastases
boolean
C0002594 (UMLS CUI [1])
transaminases in presence of hepatic metastases
Item
got and/or gpt > 2.5 x the upper normal limits in presence of hepatic metastases
boolean
C0002594 (UMLS CUI [1])
C0494165 (UMLS CUI [2])
C0494165 (UMLS CUI [2])
bilirubin
Item
bilirubin > 1.5 x the upper normal limit
boolean
C1278039 (UMLS CUI [1])
Comorbidity
Item
any concomitant pathology that would, in the investigator's opinion, contraindicate the use of the drugs in this study
boolean
C0009488 (UMLS CUI [1])
Unable Informed Consent
Item
inability to provide informed consent
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
inability to comply with follow-up
Item
inability to comply with follow-up
boolean
C3274571 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])