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Korean Hereditary Breast Cancer Study

Korean Hereditary Breast Cancer Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00595348
Acronym
KOHBRA
Enrollment
2250
Registered
2008-01-16
Start date
2007-11-30
Completion date
2017-05-31
Last updated
2011-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Ovarian Cancer

Brief summary

1. To evaluate the prevalence of BRCA1/2 mutation of breast cancer patients with family history of breast/ovarian cancer. 2. To evaluate the prevalence of BRCA1/2 mutation of breast cancer patients without family history, but high risk of hereditary cancer. 3. To evaluate the prevalence of BRCA1/2 mutation of family member of BRCA1/2 mutation. 4. To evaluate the prevalence of ovarian cancer of population of above 3 groups.

Detailed description

1. To find founder mutation in Korean 2. To correlation prevalence with risk evaluation 3. To find risk factors concerning life style

Interventions

None listed

Sponsors

Korean Breast Cancer Study Group
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Over 19 years old * Agree to this study * Breast cancer patient with family history of breast/ovarian cancer (1 subgroup) * Breast cancer patient; young age (\<40), bilateral, male, combined ovarian (2 subgroup) * Family members with 1, 2 subgroups (3 subgroup)

Exclusion criteria

* Under 20 years old * Unable to decide for oneself

Design outcomes

Primary

MeasureTime frame
Find out the prevalence of BRCA1/2 mutation of high risk breast cancer patients6 years

Countries

South Korea

Contacts

Primary ContactKu Sang Kim, M.D, AME.
ideakims@gmail.com82-31-219-5200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026