Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
OBSERVATIONAL
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
* To screen population with high risk for breast cancer
* To promote the concept and importance of surveillance mammography
* To find out the incidence of breast cancer in population who are in high risk for breast cancer
* To collect blood samples for molecular analysis
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Breast Tissue Study of Breast Diseases Among Women in Hong Kong
NCT01885039
Comprehensive Screening for Women at High Genetic Risk for Developing Breast Cancer
NCT00255060
Women At Risk: The High Risk Breast Cancer Program
NCT01034891
Hong Kong Breast Cancer Study
NCT02889458
Towards Early Detection of Breast Cancer in High Risk Population
NCT05268913
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* \> 40 years of age
* Women who have first-degree relative suffered from breast cancer
* Women who have first-degree relative suffered from ovarian cancer
* Family history of male breast cancer
* Family history of breast cancer (not necessarily first degree relatives) diagnosed before age of 40
* Family history of breast cancer (not necessarily first degree relatives) affecting 2 or more family members
* Personal history of ovarian cancer
* Personal history of premalignant conditions of breast and ovary
Exclusion Criteria
41 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Organisation for Oncology and Translational Research
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Louis WC Chow
Role: PRINCIPAL_INVESTIGATOR
UNIMED Medical Institute
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
UNIMED Medical Institute
Wan Chai, , Hong Kong
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OOTR-SBR001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.