Informatie:
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ID
26091
Beschrijving
Axillary Sentinel Lymph Node Detection in Breast Cancers > 2 cm; ODM derived from: https://clinicaltrials.gov/show/NCT00636467
Link
https://clinicaltrials.gov/show/NCT00636467
Trefwoorden
Versies (1)
- 09-10-17 09-10-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
9 oktober 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00636467
Eligibility Breast Cancer NCT00636467
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00636467
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Gender | Age
Item
female, age ≥ 18 years
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Invasive carcinoma of breast Unifocal | Tumor size | Examination clinical | Imaging
Item
patient with invasive unifocal breast cancer with tumor size > 2 cm at initial examination (clinical examination and/or imaging)
boolean
C0853879 (UMLS CUI [1,1])
C0443337 (UMLS CUI [1,2])
C0475440 (UMLS CUI [2])
C1456356 (UMLS CUI [3])
C0011923 (UMLS CUI [4])
C0443337 (UMLS CUI [1,2])
C0475440 (UMLS CUI [2])
C1456356 (UMLS CUI [3])
C0011923 (UMLS CUI [4])
Pre-op diagnosis Invasive carcinoma of breast
Item
preoperative histological diagnosis of infiltrating mammary carcinoma
boolean
C1318968 (UMLS CUI [1,1])
C0853879 (UMLS CUI [1,2])
C0853879 (UMLS CUI [1,2])
Lymph nodes Absent Clinical examination
Item
no lymph node at clinical examination
boolean
C0024204 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C1456356 (UMLS CUI [1,3])
C0332197 (UMLS CUI [1,2])
C1456356 (UMLS CUI [1,3])
Cancer treatment Absent | Operative Surgical Procedures Status pre-
Item
no treatment for this cancer before surgery
boolean
C0920425 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
C0332197 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
Affiliation Social security systems
Item
mandatory affiliation with a social security system
boolean
C1510825 (UMLS CUI [1,1])
C2371809 (UMLS CUI [1,2])
C2371809 (UMLS CUI [1,2])
Informed Consent
Item
written, signed informed consent
boolean
C0021430 (UMLS CUI [1])
Invasive carcinoma of breast
Item
no invasive breast cancer
boolean
C0853879 (UMLS CUI [1])
Breast Carcinoma Size
Item
breast tumor =< 2 cm
boolean
C0678222 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,2])
Pre-op diagnosis Except Invasive carcinoma of breast
Item
preoperative histological diagnosis other than infiltrating mammary carcinoma
boolean
C1318968 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C0853879 (UMLS CUI [1,3])
C0332300 (UMLS CUI [1,2])
C0853879 (UMLS CUI [1,3])
Multifocal breast carcinoma
Item
multifocal breast cancer
boolean
C2986662 (UMLS CUI [1])
Inflammatory Breast Carcinoma
Item
inflammatory breast cancer
boolean
C0278601 (UMLS CUI [1])
Neoplasm Metastasis
Item
metastatic cancer
boolean
C0027627 (UMLS CUI [1])
Operation on breast Ipsilateral
Item
history of homolateral breast surgery
boolean
C3714726 (UMLS CUI [1,1])
C0441989 (UMLS CUI [1,2])
C0441989 (UMLS CUI [1,2])
Hypersensitivity
Item
history of allergic disorders
boolean
C0020517 (UMLS CUI [1])
Breast Carcinoma Ipsilateral
Item
history of homolateral breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0441989 (UMLS CUI [1,2])
C0441989 (UMLS CUI [1,2])
Follow-up Difficult
Item
difficult follow-up
boolean
C3274571 (UMLS CUI [1,1])
C0332218 (UMLS CUI [1,2])
C0332218 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating woman
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
previous inclusion in the trial
boolean
C2348568 (UMLS CUI [1])