Informatie:
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ID
27290
Beschrijving
Trial Comparing Prone and Supine Intensity-modulated Radiotherapy (IMRT) After Breast-conserving Surgery in Patients With Large Breast Volume at High Risk for Skin Toxicity and Fibrosis; ODM derived from: https://clinicaltrials.gov/show/NCT00887523
Link
https://clinicaltrials.gov/show/NCT00887523
Trefwoorden
Versies (1)
- 07-11-17 07-11-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
7 november 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Breast Carcinoma NCT00887523
Eligibility Breast Carcinoma NCT00887523
- StudyEvent: Eligibility
Similar models
Eligibility Breast Carcinoma NCT00887523
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Gender
Item
female patients
boolean
C0079399 (UMLS CUI [1])
Whole Breast Irradiation Adjuvant | Lumpectomy (breast cancer)
Item
multidisciplinary decision of adjuvant whole-breast irradiation (wbi) after lumpectomy for breast cancer
boolean
C3897169 (UMLS CUI [1,1])
C1522673 (UMLS CUI [1,2])
C0740370 (UMLS CUI [2])
C1522673 (UMLS CUI [1,2])
C0740370 (UMLS CUI [2])
Age Minimum
Item
minimum 18 years
boolean
C0001779 (UMLS CUI [1,1])
C1524031 (UMLS CUI [1,2])
C1524031 (UMLS CUI [1,2])
Informed Consent
Item
informed consent obtained, signed and dated before specific protocol procedures
boolean
C0021430 (UMLS CUI [1])
Mastectomy
Item
mastectomy
boolean
C0024881 (UMLS CUI [1])
Irradiation of axillary lymph nodes Patient need for
Item
need for axillary irradiation
boolean
C2169036 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
C0686904 (UMLS CUI [1,2])
Irradiation of breast Bilateral
Item
bilateral breast irradiation
boolean
C2148528 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
C0238767 (UMLS CUI [1,2])
Prior radiation therapy
Item
previous irradiation at the same time
boolean
C0279134 (UMLS CUI [1])
Mental condition Impairing Patient | Study Protocol Comprehension Unable
Item
mental condition rendering the patient unable to understand the nature, scope and possible consequences of the study
boolean
C3840291 (UMLS CUI [1,1])
C0221099 (UMLS CUI [1,2])
C0030705 (UMLS CUI [1,3])
C2348563 (UMLS CUI [2,1])
C0162340 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0221099 (UMLS CUI [1,2])
C0030705 (UMLS CUI [1,3])
C2348563 (UMLS CUI [2,1])
C0162340 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
Protocol Compliance Unlikely | Uncooperative attitude | Follow-up visit Unable | Completion of clinical trial Unlikely
Item
patient unlikely to comply with the protocol; i.e. uncooperative attitude, inability to return for follow-up visits, and unlikely to complete the study.
boolean
C0525058 (UMLS CUI [1,1])
C0750558 (UMLS CUI [1,2])
C2188045 (UMLS CUI [2])
C0589121 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
C2732579 (UMLS CUI [4,1])
C0750558 (UMLS CUI [4,2])
C0750558 (UMLS CUI [1,2])
C2188045 (UMLS CUI [2])
C0589121 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
C2732579 (UMLS CUI [4,1])
C0750558 (UMLS CUI [4,2])