ID
36845
Description
Hypofractionation With Simultaneous Integrated Boost for Early Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01948726 Hypofractionation with simultaneous integrated boost has been investigated in a few trials and appears to be safe and feasible with less lung toxicity in smaller studies. Investigators initiated this multicenter phase II prospective trial to analyse acute toxicity of hypofractionation with simultaneous integrated boost in patients with early breast cancer under the hypothesis that the ratio of patients with acute radiogenic toxicity Grad II according NCI-CTCAE amounts maximum 20%.
Link
https://clinicaltrials.gov/show/NCT01948726
Keywords
Versions (1)
- 6/15/19 6/15/19 -
Copyright Holder
University of Schleswig-Holstein
Uploaded on
June 15, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Hypofractionation for Breast Cancer NCT01948726
Eligibility Criteria
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Mastectomy
Data type
boolean
Alias
- UMLS CUI [1]
- C0024881
Description
No Boost radiation indication
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0521090
- UMLS CUI [1,2]
- C2919491
Description
Positive resection margins or insufficient boost volume identification
Data type
boolean
Alias
- UMLS CUI [1]
- C1709603
- UMLS CUI [2,1]
- C0231180
- UMLS CUI [2,2]
- C0205396
- UMLS CUI [2,3]
- C2919491
- UMLS CUI [2,4]
- C0449468
Description
Regional lymph node radiotherapy indication
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0729852
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C1522449
Description
History of breast or thorax radiotherapy
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0241889
- UMLS CUI [1,2]
- C0948310
- UMLS CUI [2,1]
- C0241889
- UMLS CUI [2,2]
- C4038705
Description
Extended postoperative seroma
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0231449
- UMLS CUI [1,2]
- C1998103
- UMLS CUI [1,3]
- C0439659
- UMLS CUI [1,4]
- C1522449
Description
Mental disorder affecting compliance
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0004936
- UMLS CUI [1,2]
- C0392760
- UMLS CUI [1,3]
- C4319828
- UMLS CUI [2,1]
- C0848775
- UMLS CUI [2,2]
- C0392760
- UMLS CUI [2,3]
- C4319828
Description
Pregnancy, Lactation or Childbearing potential
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C2828358
- UMLS CUI [3,1]
- C3831118
- UMLS CUI [3,2]
- C0332268
- UMLS CUI [3,3]
- C0700589
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Eligibility Criteria
- StudyEvent: Eligibility
C0521091 (UMLS CUI [1,2])
C0006142 (UMLS CUI [1,3])
C0917927 (UMLS CUI [1,4])
C1709157 (UMLS CUI [1,5])
C0242939 (UMLS CUI [1,2])
C2919491 (UMLS CUI [1,3])
C0205396 (UMLS CUI [1,2])
C0677930 (UMLS CUI [1,3])
C0181739 (UMLS CUI [1,4])
C0175722 (UMLS CUI [1,5])
C0205225 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C0917927 (UMLS CUI [1,4])
C0332288 (UMLS CUI [1,5])
C0513965 (UMLS CUI [1,6])
C0279025 (UMLS CUI [1,2])
C0032790 (UMLS CUI [1,3])
C0445204 (UMLS CUI [1,4])
C0521104 (UMLS CUI [1,5])
C3146298 (UMLS CUI [1,6])
C2919491 (UMLS CUI [1,2])
C0231180 (UMLS CUI [2,1])
C0205396 (UMLS CUI [2,2])
C2919491 (UMLS CUI [2,3])
C0449468 (UMLS CUI [2,4])
C0392360 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
C0948310 (UMLS CUI [1,2])
C0241889 (UMLS CUI [2,1])
C4038705 (UMLS CUI [2,2])
C1998103 (UMLS CUI [1,2])
C0439659 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,4])
C0392760 (UMLS CUI [1,2])
C4319828 (UMLS CUI [1,3])
C0848775 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C4319828 (UMLS CUI [2,3])
C2828358 (UMLS CUI [2])
C3831118 (UMLS CUI [3,1])
C0332268 (UMLS CUI [3,2])
C0700589 (UMLS CUI [3,3])