ID

43717

Description

Studying Breast Cancer Risk in Women Who Are BRCA1/BRCA2 Mutation Carriers; ODM derived from: https://clinicaltrials.gov/show/NCT00897455

Lien

https://clinicaltrials.gov/show/NCT00897455

Mots-clés

  1. 02/10/2017 02/10/2017 -
  2. 04/10/2017 04/10/2017 -
  3. 20/09/2021 20/09/2021 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility brca1 Mutation Carrier NCT00897455

Eligibility brca1 Mutation Carrier NCT00897455

Criteria
Description

Criteria

known positive brca1/brca2 mutation carrier
Description

BRCA1 Mutation Carrier Positive | BRCA2 Mutation Carrier Positive

Type de données

boolean

Alias
UMLS CUI [1,1]
C3899965
UMLS CUI [1,2]
C1514241
UMLS CUI [2,1]
C3899964
UMLS CUI [2,2]
C1514241
with or without a personal history of breast cancer prior to enrollment in clinical trial gog-0199
Description

Breast Carcinoma Personal History | Breast Carcinoma Personal History Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0262926
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C0262926
UMLS CUI [2,3]
C0332197
currently enrolled in clinical trial gog-0199 and meets the following criteria:
Description

Enrollment Clinical Trial Specified

Type de données

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0205369
completed baseline questionnaire (bq-199)
Description

Baseline Questionnaire Completed

Type de données

boolean

Alias
UMLS CUI [1,1]
C1442488
UMLS CUI [1,2]
C0034394
UMLS CUI [1,3]
C0205197
provided information on prior breast cancer history, including date of diagnosis
Description

Information Breast Carcinoma Medical History | Date of diagnosis

Type de données

boolean

Alias
UMLS CUI [1,1]
C1533716
UMLS CUI [1,2]
C0678222
UMLS CUI [1,3]
C0262926
UMLS CUI [2]
C2316983
provided complete data from the dna analysis on the genetic variants of interest
Description

DNA analysis Variants Genetic

Type de données

boolean

Alias
UMLS CUI [1,1]
C0200898
UMLS CUI [1,2]
C0205419
UMLS CUI [1,3]
C0314603
signed an approved informed consent and authorization permitting release of personal health information
Description

Informed Consent | Availability of Personal Health Information

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0470187
UMLS CUI [2,2]
C4045976
hormone receptor status not specified
Description

Hormone Receptor Status Unspecified

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205370
patient characteristics:
Description

Client Characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
menopausal status not specified
Description

Menopausal Status Unspecified

Type de données

boolean

Alias
UMLS CUI [1,1]
C3829127
UMLS CUI [1,2]
C0205370
prior concurrent therapy:
Description

Therapeutic procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Description

ID.12

Type de données

boolean

Similar models

Eligibility brca1 Mutation Carrier NCT00897455

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
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])
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])
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])
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])
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])
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])
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])
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])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.12
Item
see disease characteristics
boolean

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