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Información:
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ID
26007
Descripción
Studying Breast Cancer Risk in Women Who Are BRCA1/BRCA2 Mutation Carriers; ODM derived from: https://clinicaltrials.gov/show/NCT00897455
Link
https://clinicaltrials.gov/show/NCT00897455
Palabras clave
Versiones (3)
- 2/10/17 2/10/17 -
- 4/10/17 4/10/17 -
- 20/9/21 20/9/21 -
Titular de derechos de autor
See clinicaltrials.gov
Subido en
4 de octubre de 2017
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility brca1 Mutation Carrier NCT00897455
Eligibility brca1 Mutation Carrier NCT00897455
- StudyEvent: Eligibility
Similar models
Eligibility brca1 Mutation Carrier NCT00897455
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
BRCA1 Mutation Carrier Positive | BRCA2 Mutation Carrier Positive
Item
known positive brca1/brca2 mutation carrier
boolean
C3899965 (UMLS CUI [1,1])
C1514241 (UMLS CUI [1,2])
C3899964 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])
C1514241 (UMLS CUI [1,2])
C3899964 (UMLS CUI [2,1])
C1514241 (UMLS CUI [2,2])
Breast Carcinoma Personal History | Breast Carcinoma Personal History Absent
Item
with or without a personal history of breast cancer prior to enrollment in clinical trial gog-0199
boolean
C0678222 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0262926 (UMLS CUI [1,2])
C0678222 (UMLS CUI [2,1])
C0262926 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Enrollment Clinical Trial Specified
Item
currently enrolled in clinical trial gog-0199 and meets the following criteria:
boolean
C1516879 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Baseline Questionnaire Completed
Item
completed baseline questionnaire (bq-199)
boolean
C1442488 (UMLS CUI [1,1])
C0034394 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C0034394 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Information Breast Carcinoma Medical History | Date of diagnosis
Item
provided information on prior breast cancer history, including date of diagnosis
boolean
C1533716 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
C2316983 (UMLS CUI [2])
C0678222 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
C2316983 (UMLS CUI [2])
DNA analysis Variants Genetic
Item
provided complete data from the dna analysis on the genetic variants of interest
boolean
C0200898 (UMLS CUI [1,1])
C0205419 (UMLS CUI [1,2])
C0314603 (UMLS CUI [1,3])
C0205419 (UMLS CUI [1,2])
C0314603 (UMLS CUI [1,3])
Informed Consent | Availability of Personal Health Information
Item
signed an approved informed consent and authorization permitting release of personal health information
boolean
C0021430 (UMLS CUI [1])
C0470187 (UMLS CUI [2,1])
C4045976 (UMLS CUI [2,2])
C0470187 (UMLS CUI [2,1])
C4045976 (UMLS CUI [2,2])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C1513126 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.12
Item
see disease characteristics
boolean