Informationen: Aufgrund von gesteigerten Botaktivitäten, waren wir leider gezwungen, die Suche hinter einen Login zu stellen. Links zu Formularen können weiterhin mit anderen geteilt und ohne Login angeschaut werden. Vielen Dank für Ihr Verständnis.
Informationen:
Fehler:
ID
43540
Beschreibung
Side Effects Involving the Heart in Women With Breast Cancer Receiving Doxorubicin and Trastuzumab; ODM derived from: https://clinicaltrials.gov/show/NCT00875238
Link
https://clinicaltrials.gov/show/NCT00875238
Stichworte
Versionen (2)
- 23.10.17 23.10.17 -
- 20.09.21 20.09.21 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
20. September 2021
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 NCT00875238
Eligibility Breast Cancer NCT00875238
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT00875238
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Breast Carcinoma
Item
diagnosed with breast cancer
boolean
C0678222 (UMLS CUI [1])
Therapeutic procedure Oncology Center
Item
receiving treatment at vanderbilt ingram cancer center and other participating oncology practices in middle tennessee and southern kentucky
boolean
C0087111 (UMLS CUI [1,1])
C1552534 (UMLS CUI [1,2])
C1552534 (UMLS CUI [1,2])
Doxorubicin Hydrochloride Course Quantity
Item
starting a standard doxorubicin hydrochloride regimen for 4 courses
boolean
C0546861 (UMLS CUI [1,1])
C0750729 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0750729 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Trastuzumab Scheduled
Item
also scheduled to receive trastuzumab (for patients enrolled in sub-study b only)
boolean
C0728747 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,2])
Neoplasm Metastasis Absent
Item
no presence of metastatic disease
boolean
C0027627 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,2])
Karnofsky Performance Status
Item
karnofsky performance status 60-100%
boolean
C0206065 (UMLS CUI [1])
Pregnancy Absent
Item
not pregnant
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,2])
Pregnancy test negative
Item
negative pregnancy test
boolean
C0427780 (UMLS CUI [1])
Criteria Additional | MRI
Item
additional criteria for sub-study a (mri):
boolean
C0243161 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C0024485 (UMLS CUI [2])
C1524062 (UMLS CUI [1,2])
C0024485 (UMLS CUI [2])
Glomerular Filtration Rate
Item
glomerular filtration rate ≥ 60 ml/min
boolean
C0017654 (UMLS CUI [1])
Exclusion Criteria | Implanted medical device Electronic | Cochlear Implants | metallic implant | Shrapnel | Clips Neurosurgical Procedures
Item
no implanted electronic devices, cochlear implants, metallic implants, shrapnel or neurosurgical clips
boolean
C0680251 (UMLS CUI [1])
C2735362 (UMLS CUI [2,1])
C0013850 (UMLS CUI [2,2])
C0009199 (UMLS CUI [3])
C3693688 (UMLS CUI [4])
C0522670 (UMLS CUI [5])
C0038917 (UMLS CUI [6,1])
C0524850 (UMLS CUI [6,2])
C2735362 (UMLS CUI [2,1])
C0013850 (UMLS CUI [2,2])
C0009199 (UMLS CUI [3])
C3693688 (UMLS CUI [4])
C0522670 (UMLS CUI [5])
C0038917 (UMLS CUI [6,1])
C0524850 (UMLS CUI [6,2])
Exclusion | Adverse reaction Gadolinium-based Contrast Agent
Item
no prior adverse reaction to gadolinium-based contrast agents
boolean
C2828389 (UMLS CUI [1])
C0559546 (UMLS CUI [2,1])
C3249258 (UMLS CUI [2,2])
C0559546 (UMLS CUI [2,1])
C3249258 (UMLS CUI [2,2])
Normal weight | Normal height | Patient Appropriate MRI Scanner
Item
must not exceed the weight limit or be too large to fit in the mri scanner
boolean
C2712185 (UMLS CUI [1])
C0587053 (UMLS CUI [2])
C0030705 (UMLS CUI [3,1])
C1548787 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
C1710020 (UMLS CUI [3,4])
C0587053 (UMLS CUI [2])
C0030705 (UMLS CUI [3,1])
C1548787 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
C1710020 (UMLS CUI [3,4])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.18
Item
see disease characteristics
boolean
Exclusion | Anthracyclines
Item
no prior anthracycline chemotherapy
boolean
C2828389 (UMLS CUI [1])
C0282564 (UMLS CUI [2])
C0282564 (UMLS CUI [2])