ID

38046

Description

Feasibility Study for the Determination of Oxysterols in Patients With Breast Cancer Receiving Hormonal Therapy With Tamoxifen or Not; ODM derived from: https://clinicaltrials.gov/show/NCT01553903

Link

https://clinicaltrials.gov/show/NCT01553903

Keywords

Versions (2)
  1. 9/11/19 9/11/19 -
  2. 9/12/19 9/12/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 12, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01553903

English

Eligibility Breast Cancer NCT01553903

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. women of more than 18 years old (menopause or not).
Description

Gender | Age | Menopause | Menopause Absent

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
UMLS CUI [3]
C0025320
UMLS CUI [4,1]
C0025320
UMLS CUI [4,2]
C0332197
2. women with invasive breast cancer metastatic or non-metastatic, for which treatment with tamoxifen or anti-aromatase is retained.
Description

Gender | Invasive carcinoma of breast metastatic | Invasive carcinoma of breast | Tamoxifen | Aromatase Inhibitors

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0853879
UMLS CUI [2,2]
C1522484
UMLS CUI [3]
C0853879
UMLS CUI [4]
C0039286
UMLS CUI [5]
C0593802
3. cancer hormone-expressing estrogen receptor (er) and / or progesterone receptor (pr) (≥ 10% of tumor cells in technical hic).
Description

Cancer Hormone Expression Estrogen Receptor | Cancer Hormone Expression Progesterone Receptor | Tumor Cells Percentage Immunohistochemistry

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0019932
UMLS CUI [1,3]
C0017262
UMLS CUI [1,4]
C0034804
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0019932
UMLS CUI [2,3]
C0017262
UMLS CUI [2,4]
C0034833
UMLS CUI [3,1]
C0597032
UMLS CUI [3,2]
C0439165
UMLS CUI [3,3]
C0021044
4. any previous hormonal therapy, stopped for progression, should be discontinued for at least 21 days prior to study entry.
Description

Hormone Therapy To be stopped

Data type

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C1272691
5. who ≤ 2.
Description

WHO performance status scale

Data type

boolean

Alias
UMLS CUI [1]
C1298650
6. women of childbearing age must use effective contraception for the duration of the study.
Description

Childbearing Potential Contraceptive methods

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
7. informed consent obtained and signed before any specific procedure in the study.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
8. patient member in a national insurance scheme.
Description

Patient Member National Health Insurance

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0680022
UMLS CUI [1,3]
C0027452
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patient with breast cancer her2 positive (ihc and / or fish-cish)
Description

HER2-positive carcinoma of breast Immunohistochemistry | HER2-positive carcinoma of breast FISH | HER2-positive carcinoma of breast CISH

Data type

boolean

Alias
UMLS CUI [1,1]
C1960398
UMLS CUI [1,2]
C0021044
UMLS CUI [2,1]
C1960398
UMLS CUI [2,2]
C0162789
UMLS CUI [3,1]
C1960398
UMLS CUI [3,2]
C1516514
2. patient already receiving hormonal therapy or patient who has not stopped hormonal therapy for at least 21 days.
Description

Hormone Therapy Pre-existing | Discontinuation Hormone Therapy Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C2347662
UMLS CUI [2,1]
C1444662
UMLS CUI [2,2]
C0279025
UMLS CUI [2,3]
C0332268
3. patient that should receive a chemotherapy and / or another targeted therapy (other than hormonal therapy) for the treatment of the breast cancer.
Description

Chemotherapy Required Breast Carcinoma | Targeted Therapy Required Breast Carcinoma | Exception Hormone Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0678222
UMLS CUI [2,1]
C2985566
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0678222
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0279025
4. any other medical or psychiatric condition or laboratory abnormality severe, acute or chronic making the inclusion of the patient in the study inappropriate in the opinion of the investigator.
Description

Medical condition Study Subject Participation Status Inappropriate | Mental condition Study Subject Participation Status Inappropriate | Laboratory test result abnormal Severe Study Subject Participation Status Inappropriate | Laboratory test result abnormal Study Subject Participation Status Inappropriate | Laboratory test result abnormal chronic Study Subject Participation Status Inappropriate

Data type

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C1548788
UMLS CUI [2,1]
C3840291
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C1548788
UMLS CUI [3,1]
C0438215
UMLS CUI [3,2]
C0205082
UMLS CUI [3,3]
C2348568
UMLS CUI [3,4]
C1548788
UMLS CUI [4,1]
C0438215
UMLS CUI [4,2]
C2348568
UMLS CUI [4,3]
C1548788
UMLS CUI [5,1]
C0438215
UMLS CUI [5,2]
C0205191
UMLS CUI [5,3]
C2348568
UMLS CUI [5,4]
C1548788
5. patient unable to follow procedures, visits, examinations described in the study.
Description

Protocol Compliance Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
6. pregnant women or nursing mothers can not participate in the study.
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
7. patients under legal guardianship.
Description

Patients Guardianship

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0870627
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Similar models

Eligibility Breast Cancer NCT01553903

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age | Menopause | Menopause Absent
Item
1. women of more than 18 years old (menopause or not).
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0025320 (UMLS CUI [3])
C0025320 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Gender | Invasive carcinoma of breast metastatic | Invasive carcinoma of breast | Tamoxifen | Aromatase Inhibitors
Item
2. women with invasive breast cancer metastatic or non-metastatic, for which treatment with tamoxifen or anti-aromatase is retained.
boolean
C0079399 (UMLS CUI [1])
C0853879 (UMLS CUI [2,1])
C1522484 (UMLS CUI [2,2])
C0853879 (UMLS CUI [3])
C0039286 (UMLS CUI [4])
C0593802 (UMLS CUI [5])
Cancer Hormone Expression Estrogen Receptor | Cancer Hormone Expression Progesterone Receptor | Tumor Cells Percentage Immunohistochemistry
Item
3. cancer hormone-expressing estrogen receptor (er) and / or progesterone receptor (pr) (≥ 10% of tumor cells in technical hic).
boolean
C0006826 (UMLS CUI [1,1])
C0019932 (UMLS CUI [1,2])
C0017262 (UMLS CUI [1,3])
C0034804 (UMLS CUI [1,4])
C0006826 (UMLS CUI [2,1])
C0019932 (UMLS CUI [2,2])
C0017262 (UMLS CUI [2,3])
C0034833 (UMLS CUI [2,4])
C0597032 (UMLS CUI [3,1])
C0439165 (UMLS CUI [3,2])
C0021044 (UMLS CUI [3,3])
Hormone Therapy To be stopped
Item
4. any previous hormonal therapy, stopped for progression, should be discontinued for at least 21 days prior to study entry.
boolean
C0279025 (UMLS CUI [1,1])
C1272691 (UMLS CUI [1,2])
WHO performance status scale
Item
5. who ≤ 2.
boolean
C1298650 (UMLS CUI [1])
Childbearing Potential Contraceptive methods
Item
6. women of childbearing age must use effective contraception for the duration of the study.
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Informed Consent
Item
7. informed consent obtained and signed before any specific procedure in the study.
boolean
C0021430 (UMLS CUI [1])
Patient Member National Health Insurance
Item
8. patient member in a national insurance scheme.
boolean
C0030705 (UMLS CUI [1,1])
C0680022 (UMLS CUI [1,2])
C0027452 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
HER2-positive carcinoma of breast Immunohistochemistry | HER2-positive carcinoma of breast FISH | HER2-positive carcinoma of breast CISH
Item
1. patient with breast cancer her2 positive (ihc and / or fish-cish)
boolean
C1960398 (UMLS CUI [1,1])
C0021044 (UMLS CUI [1,2])
C1960398 (UMLS CUI [2,1])
C0162789 (UMLS CUI [2,2])
C1960398 (UMLS CUI [3,1])
C1516514 (UMLS CUI [3,2])
Hormone Therapy Pre-existing | Discontinuation Hormone Therapy Lacking
Item
2. patient already receiving hormonal therapy or patient who has not stopped hormonal therapy for at least 21 days.
boolean
C0279025 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
C1444662 (UMLS CUI [2,1])
C0279025 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
Chemotherapy Required Breast Carcinoma | Targeted Therapy Required Breast Carcinoma | Exception Hormone Therapy
Item
3. patient that should receive a chemotherapy and / or another targeted therapy (other than hormonal therapy) for the treatment of the breast cancer.
boolean
C0392920 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C2985566 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0678222 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0279025 (UMLS CUI [3,2])
Medical condition Study Subject Participation Status Inappropriate | Mental condition Study Subject Participation Status Inappropriate | Laboratory test result abnormal Severe Study Subject Participation Status Inappropriate | Laboratory test result abnormal Study Subject Participation Status Inappropriate | Laboratory test result abnormal chronic Study Subject Participation Status Inappropriate
Item
4. any other medical or psychiatric condition or laboratory abnormality severe, acute or chronic making the inclusion of the patient in the study inappropriate in the opinion of the investigator.
boolean
C3843040 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C3840291 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C1548788 (UMLS CUI [2,3])
C0438215 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C2348568 (UMLS CUI [3,3])
C1548788 (UMLS CUI [3,4])
C0438215 (UMLS CUI [4,1])
C2348568 (UMLS CUI [4,2])
C1548788 (UMLS CUI [4,3])
C0438215 (UMLS CUI [5,1])
C0205191 (UMLS CUI [5,2])
C2348568 (UMLS CUI [5,3])
C1548788 (UMLS CUI [5,4])
Protocol Compliance Unable
Item
5. patient unable to follow procedures, visits, examinations described in the study.
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
6. pregnant women or nursing mothers can not participate in the study.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Patients Guardianship
Item
7. patients under legal guardianship.
boolean
C0030705 (UMLS CUI [1,1])
C0870627 (UMLS CUI [1,2])
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