Informationen:
Fehler:
ID
20417
Beschreibung
Radiation Therapy With or Without Temozolomide in Treating Women With Brain Metastases and Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00875355
Link
https://clinicaltrials.gov/show/NCT00875355
Stichworte
Versionen (1)
- 22.02.17 22.02.17 -
Hochgeladen am
22. Februar 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 NCT00875355
Eligibility Breast Cancer NCT00875355
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT00875355
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
breast carcinoma
Item
diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
unresectable disease or patient refused surgery
Item
unresectable disease or patient refused surgery
boolean
C1336869 (UMLS CUI [1])
C0749192 (UMLS CUI [2])
C0749192 (UMLS CUI [2])
brain metastases
Item
must have brain metastases
boolean
C0220650 (UMLS CUI [1])
characteristics
Item
patient characteristics:
boolean
C1521970 (UMLS CUI [1])
who performance status
Item
who performance status 0-2
boolean
C1298651 (UMLS CUI [1])
anc
Item
anc ≥ 1,500/mm³
boolean
C0948762 (UMLS CUI [1])
platelet count
Item
platelet count ≥ 100,000/mm³
boolean
C0005821 (UMLS CUI [1])
liver transaminases
Item
liver transaminases ≤ 1.5 times upper limit of normal (uln)
boolean
C1856363 (UMLS CUI [1])
creatinine
Item
creatinine < 1.5 times uln
boolean
C0201976 (UMLS CUI [1])
not pregnant or nursing
Item
not pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0085537 (UMLS CUI [2])
C0085537 (UMLS CUI [2])
Contraceptive methods; Childbearing Potential
Item
fertile patients must use effective contraception
boolean
C0700589 (UMLS CUI [1,1])
C3831118 (UMLS CUI [1,2])
C3831118 (UMLS CUI [1,2])
carcinomatous meningitis
Item
no carcinomatous meningitis
boolean
C0220654 (UMLS CUI [1])
History of neoplastic disease | Basal cell carcinoma | Carcinoma in situ of uterine cervix
Item
no history of cancer except for basal cell carcinoma of the skin or carcinoma in situ of the cervix
boolean
C2735088 (UMLS CUI [1])
C0007117 (UMLS CUI [2])
C0851140 (UMLS CUI [3])
C0007117 (UMLS CUI [2])
C0851140 (UMLS CUI [3])
comorbidity limited protocol compliance
Item
no other serious concurrent disease that is, in the opinion of the investigator, likely to interfere with study evaluation and treatment
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
no contraindications to treatment with temozolomide
Item
no contraindications to treatment with temozolomide
boolean
C0076080 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C1301624 (UMLS CUI [1,2])
limited protocol compliance
Item
no psychological, familial, social, or geographic situations that preclude clinical follow up
boolean
C0439801 (UMLS CUI [1,1])
C0525058 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,2])
guardianship
Item
no patient deprived of liberty or under guardianship
boolean
C0870627 (UMLS CUI [1])
prior concurrent therapy
Item
prior concurrent therapy:
boolean
C1514463 (UMLS CUI [1,1])
C0009429 (UMLS CUI [1,2])
C0009429 (UMLS CUI [1,2])
prior brain radiotherapy
Item
no prior brain radiotherapy
boolean
C0948319 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C1514463 (UMLS CUI [1,2])
prior chemotherapy
Item
at least 10 days since prior chemotherapy
boolean
C1514457 (UMLS CUI [1])