Informationen:
Fehler:
ID
38363
Beschreibung
Fluorescence-guided Resection in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01110954
Link
https://clinicaltrials.gov/show/NCT01110954
Stichworte
Versionen (1)
- 12.10.19 12.10.19 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
12. Oktober 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 Tumour NCT01110954
Eligibility Breast Tumour NCT01110954
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Tumour NCT01110954
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Caucasian | Gender | Postmenopausal state
Item
caucasian female postmenopausal patients
boolean
C0043157 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
C0079399 (UMLS CUI [2])
C0232970 (UMLS CUI [3])
Breast Carcinoma Palpable TNM Breast tumor staging | Breast Carcinoma Non-Palpable TNM Breast tumor staging | Tumor size
Item
patients with histologically confirmed primary palpable and nonpalpable breast cancer sized up to 5 cm (t1 - t2)
boolean
C0678222 (UMLS CUI [1,1])
C0522499 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
C0678222 (UMLS CUI [2,1])
C4086626 (UMLS CUI [2,2])
C0474926 (UMLS CUI [2,3])
C0475440 (UMLS CUI [3])
C0522499 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
C0678222 (UMLS CUI [2,1])
C4086626 (UMLS CUI [2,2])
C0474926 (UMLS CUI [2,3])
C0475440 (UMLS CUI [3])
Neoplasm Metastasis Suspicious TNM clinical staging
Item
suspicious lymphogenic metastases (cn1-3)
boolean
C0027627 (UMLS CUI [1,1])
C0750493 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
C0750493 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,3])
Liver disease | Chronic liver disease
Item
acute or chronic hepatic diseases
boolean
C0023895 (UMLS CUI [1])
C0341439 (UMLS CUI [2])
C0341439 (UMLS CUI [2])
Kidney Disease | Renal dysfunction
Item
manifest renal diseases with renal dysfunction
boolean
C0022658 (UMLS CUI [1])
C3279454 (UMLS CUI [2])
C3279454 (UMLS CUI [2])
Heart Disease
Item
relevant cardiac disease
boolean
C0018799 (UMLS CUI [1])
Investigational Therapy Breast Carcinoma
Item
preceding therapy of breast tumour under investigation
boolean
C0949266 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,2])
Hooked wire Placement Attempt
Item
patients with multiple attempts of hook-wire placement in preparation of surgery
boolean
C0441180 (UMLS CUI [1,1])
C0589567 (UMLS CUI [1,2])
C1516084 (UMLS CUI [1,3])
C0589567 (UMLS CUI [1,2])
C1516084 (UMLS CUI [1,3])
Dementia Interferes with Comprehension Study Protocol | Mental condition Interferes with Comprehension Study Protocol | Dementia Interferes with Informed Consent | Mental condition Interferes with Informed Consent
Item
dementia or psychic condition that might interfere with the ability to understand the study and thus give a written informed consent
boolean
C0497327 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0162340 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
C3840291 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C2348563 (UMLS CUI [2,4])
C0497327 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0021430 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C0021430 (UMLS CUI [4,3])
C0521102 (UMLS CUI [1,2])
C0162340 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
C3840291 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0162340 (UMLS CUI [2,3])
C2348563 (UMLS CUI [2,4])
C0497327 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0021430 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C0021430 (UMLS CUI [4,3])
Study Subject Participation Status
Item
simultaneous participation in another clinical study or participation in another clinical study in the 30 days directly preceding treatment
boolean
C2348568 (UMLS CUI [1])