ID
12833
Description
Hypofractionated Radiotherapy Post-Lumpectomy in Women With Node Negative Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00156052
Link
https://clinicaltrials.gov/show/NCT00156052
Keywords
Versions (1)
- 12/29/15 12/29/15 -
Uploaded on
December 29, 2015
DOI
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License
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00156052
Eligibility Breast Cancer NCT00156052
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
1. tumour greater than 5 cm in greatest diameter on pathological examination.
Data type
boolean
Alias
- UMLS CUI [1]
- C0475440
Description
2. the presence of invasive or intraductal (noninvasive) breast cancer involving the surgical margins.
Data type
boolean
Alias
- UMLS CUI [1]
- C0808133
Description
3. clinical evidence prior to surgery of infiltration of the skin of the involved breast such as edema, ulceration, or fixation of the tumour to underlying muscle, or inflammatory breast cancer.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0241076
- UMLS CUI [1,2]
- C0006141
- UMLS CUI [2]
- C0278601
Description
4. bilateral malignancy of the breast (synchronous or metachronous).
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0677861
- UMLS CUI [1,2]
- C0006141
Description
5. more than one primary invasive tumour in the same breast.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0677930
- UMLS CUI [1,2]
- C0205092
- UMLS CUI [1,3]
- C0443302
Description
6. previous surgery for breast cancer.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C3714726
- UMLS CUI [1,3]
- C0920424
Description
7. pathological status of axilla is unknown.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0443276
- UMLS CUI [1,2]
- C0004454
Description
8. status for adjuvant systemic therapy not determined.
Data type
boolean
Alias
- UMLS CUI [1]
- C1636177
Description
9. for patients not treated with adjuvant chemotherapy: unable to commence radiation therapy within 16 weeks of last surgical procedure on the breast.
Data type
boolean
Alias
- UMLS CUI [1]
- C3846110
Description
10. for patients treated with adjuvant chemotherapy: unable to commence radiation therapy within 8 weeks of the last dose of chemotherapy.
Data type
boolean
Alias
- UMLS CUI [1]
- C1522449
Description
11. serious nonmalignant disease (eg. cardiovascular, renal, etc.) which would preclude surgical or radiation treatment.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0852649
Description
12. currently pregnant or lactating.
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
13. breast deemed too large to permit satisfactory radiation (ie. separation > 25 cm).
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1522449
- UMLS CUI [1,2]
- C0541812
Description
14. previous concomitant malignancies of any type except squamous, or basal cell carcinomas of the skin, or carcinoma in situ of the cervix which have been effectively treated.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0006826
Description
15. geographic inaccessibility for follow-up.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0814423
- UMLS CUI [1,2]
- C1522577
Description
16. psychiatric or addictive disorders which preclude obtaining informed consent or adherence to the protocol.
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0439801
- UMLS CUI [1,3]
- C0009488
Similar models
Eligibility Breast Cancer NCT00156052
- StudyEvent: Eligibility
C0445092 (UMLS CUI [1,2])
C0006141 (UMLS CUI [1,2])
C0278601 (UMLS CUI [2])
C0006141 (UMLS CUI [1,2])
C0205092 (UMLS CUI [1,2])
C0443302 (UMLS CUI [1,3])
C3714726 (UMLS CUI [1,2])
C0920424 (UMLS CUI [1,3])
C0004454 (UMLS CUI [1,2])
C0852649 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0541812 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,2])
C1522577 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])