Informationen:
Fehler:
ID
38201
Beschreibung
Intraoperative Radiation Therapy in Early Stage Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02266602
Link
https://clinicaltrials.gov/show/NCT02266602
Stichworte
Versionen (1)
- 26.09.19 26.09.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
26. September 2019
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 NCT02266602
Eligibility Breast Cancer NCT02266602
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT02266602
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Inclusion criteria General
Item
general inclusion criteria
boolean
C1512693 (UMLS CUI [1,1])
C0205246 (UMLS CUI [1,2])
C0205246 (UMLS CUI [1,2])
Age
Item
1. age ≥ 45 years.
boolean
C0001779 (UMLS CUI [1])
TNM Breast tumor staging
Item
2. clinical stage tis, t1, t2 (≤ 3cm), n0, m0 (ajcc classification).
boolean
C0474926 (UMLS CUI [1])
Invasive Ductal Breast Carcinoma | Invasive Lobular Breast Carcinoma | DCIS | Pleomorphic lobular carcinoma in situ
Item
3. invasive ductal or lobular carcinoma, dcis and/ or pleomorphic lobular carcinoma in situ.
boolean
C1134719 (UMLS CUI [1])
C0279565 (UMLS CUI [2])
C0007124 (UMLS CUI [3])
C2919327 (UMLS CUI [4])
C0279565 (UMLS CUI [2])
C0007124 (UMLS CUI [3])
C2919327 (UMLS CUI [4])
Scleroderma | Systemic Sclerosis | Lupus Erythematosus
Item
1. scleroderma, systemic sclerosis and active lupus.
boolean
C0011644 (UMLS CUI [1])
C0036421 (UMLS CUI [2])
C0409974 (UMLS CUI [3])
C0036421 (UMLS CUI [2])
C0409974 (UMLS CUI [3])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
2. participation in an investigational drug or device study.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Prior radiation therapy Ipsilateral Chest | Prior radiation therapy Ipsilateral Breast
Item
3. previous ipsilateral radiation to the thorax or breast.
boolean
C0279134 (UMLS CUI [1,1])
C0441989 (UMLS CUI [1,2])
C0817096 (UMLS CUI [1,3])
C0279134 (UMLS CUI [2,1])
C0441989 (UMLS CUI [2,2])
C0006141 (UMLS CUI [2,3])
C0441989 (UMLS CUI [1,2])
C0817096 (UMLS CUI [1,3])
C0279134 (UMLS CUI [2,1])
C0441989 (UMLS CUI [2,2])
C0006141 (UMLS CUI [2,3])
Multifocal breast carcinoma
Item
4. multifocal breast cancer.
boolean
C2986662 (UMLS CUI [1])
Pregnancy
Item
5. pregnant patients.
boolean
C0032961 (UMLS CUI [1])
Informed Consent incompetent
Item
6. patient not competent to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0231190 (UMLS CUI [1,2])
C0231190 (UMLS CUI [1,2])
Neoadjuvant Therapy Systemic
Item
7. neoadjuvant systemic therapy.
boolean
C0600558 (UMLS CUI [1,1])
C0205373 (UMLS CUI [1,2])
C0205373 (UMLS CUI [1,2])
Lymphatic Invasion Biopsy
Item
8. lymphovascular invasion on biopsy pathology
boolean
C1708790 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C0005558 (UMLS CUI [1,2])