ID

27291

Description

Comparison of Set-up Reproducibility Between Prone and Supine Intensity Modulated Radiotherapy (IMRT) for the Adjuvant Treatment of Breast Carcinoma After Lumpectomy; ODM derived from: https://clinicaltrials.gov/show/NCT00887692

Link

https://clinicaltrials.gov/show/NCT00887692

Keywords

Versions (1)
  1. 11/7/17 11/7/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

November 7, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Carcinoma NCT00887692

English

Eligibility Breast Carcinoma NCT00887692

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female patients
Description

Gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
multidisciplinary decision of adjuvant radiotherapy after lumpectomy for breast cancer
Description

Radiotherapy, Adjuvant | Lumpectomy (breast cancer)

Data type

boolean

Alias
UMLS CUI [1]
C0242939
UMLS CUI [2]
C0740370
minimum 18 years
Description

Age Minimum

Data type

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C1524031
informed consent obtained, signed and dated before specific protocol procedures.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
mastectomy
Description

Mastectomy

Data type

boolean

Alias
UMLS CUI [1]
C0024881
need for axillary irradiation
Description

Irradiation of axillary lymph nodes Patient need for

Data type

boolean

Alias
UMLS CUI [1,1]
C2169036
UMLS CUI [1,2]
C0686904
bilateral breast irradiation
Description

Irradiation of breast Bilateral

Data type

boolean

Alias
UMLS CUI [1,1]
C2148528
UMLS CUI [1,2]
C0238767
previous irradiation at the same time
Description

Prior radiation therapy

Data type

boolean

Alias
UMLS CUI [1]
C0279134
pregnant or breastfeeding
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
mental condition rendering the patient unable to understand the nature, scope and possible consequences of the study.
Description

Mental condition Impairing Patient | Study Protocol Comprehension Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C3840291
UMLS CUI [1,2]
C0221099
UMLS CUI [1,3]
C0030705
UMLS CUI [2,1]
C2348563
UMLS CUI [2,2]
C0162340
UMLS CUI [2,3]
C1299582
patient unlikely to comply with the protocol; i.e. uncooperative attitude, inability to return for follow-up visits, and unlikely to complete the study.
Description

Protocol Compliance Unlikely | Uncooperative attitude | Follow-up visit Unable | Completion of clinical trial Unlikely

Data type

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0750558
UMLS CUI [2]
C2188045
UMLS CUI [3,1]
C0589121
UMLS CUI [3,2]
C1299582
UMLS CUI [4,1]
C2732579
UMLS CUI [4,2]
C0750558
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Similar models

Eligibility Breast Carcinoma NCT00887692

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
female patients
boolean
C0079399 (UMLS CUI [1])
Radiotherapy, Adjuvant | Lumpectomy (breast cancer)
Item
multidisciplinary decision of adjuvant radiotherapy after lumpectomy for breast cancer
boolean
C0242939 (UMLS CUI [1])
C0740370 (UMLS CUI [2])
Age Minimum
Item
minimum 18 years
boolean
C0001779 (UMLS CUI [1,1])
C1524031 (UMLS CUI [1,2])
Informed Consent
Item
informed consent obtained, signed and dated before specific protocol procedures.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
Irradiation of breast Bilateral
Item
bilateral breast irradiation
boolean
C2148528 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
Prior radiation therapy
Item
previous irradiation at the same time
boolean
C0279134 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
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])
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