10 Year Coronary Heart Disease (CHD) Risk Evaluation and Its Treatment Pattern Analysis in Postmenopausal Early Breast Cancer (EBC) Patients Taking Aromatase Inhibitors (AI)

NCT ID: NCT00885612

Last Updated: 2010-06-29

Study Results

Results pending

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.

Recruitment Status

COMPLETED

Total Enrollment

1114 participants

Study Classification

OBSERVATIONAL

Study Start Date

2009-05-31

Study Completion Date

2010-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

10-year CHD risk evaluation and its treatment pattern analysis in postmenopausal early breast cancer patients taking aromatase inhibitors.

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.

Breast Cancer

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Early Breast Cancer patients
* Postmenopausal Status
* patients taking Aromatase Inhibitor as adjuvant treatment no longer than 6 months

Exclusion Criteria

* Advanced Breast Cancer patients(stage iii, iv)
* Patients who are hard to be analysed by limitation of chart record according to investigators discretion
* patients who already have been registered in this study
Minimum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

AstraZeneca

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

AstraZeneca

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

JoonWoo Bahn, MD, PhD

Role: STUDY_DIRECTOR

AstraZeneca Korea

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Research Site

Cheonan, Chungcheongnam-do, South Korea

Site Status

Research Site

Chuncheon, Gangwon-do, South Korea

Site Status

Research Site

Goyang-si, Gyeonggi-do, South Korea

Site Status

Research Site

Seongnam-si, Gyeonggi-do, South Korea

Site Status

Research Site

Pohang, Gyeongsangbuk-do, South Korea

Site Status

Research Site

Masan-si, Gyeongsangnam-do, South Korea

Site Status

Research Site

Anyang, , South Korea

Site Status

Research Site

Busan, , South Korea

Site Status

Research Site

Daegu, , South Korea

Site Status

Research Site

Daejeon, , South Korea

Site Status

Research Site

Gangneung, , South Korea

Site Status

Research Site

GuangJu, , South Korea

Site Status

Research Site

Gwangju, , South Korea

Site Status

Research Site

Incheon, , South Korea

Site Status

Research Site

Inchon, , South Korea

Site Status

Research Site

Jeonju, , South Korea

Site Status

Research Site

Junam, , South Korea

Site Status

Research Site

Koyang, , South Korea

Site Status

Research Site

Kyunggi, , South Korea

Site Status

Research Site

Pusan, , South Korea

Site Status

Research Site

Seoul, , South Korea

Site Status

Research Site

Seoul(Kangbuk), , South Korea

Site Status

Research Site

Seoul(Kangdong), , South Korea

Site Status

Research Site

Seoul(Kangnam), , South Korea

Site Status

Research Site

Seoul(Yeouido), , South Korea

Site Status

Research Site

Suwon, , South Korea

Site Status

Research Site

Ulsan, , South Korea

Site Status

Countries

Review the countries where the study has at least one active or historical site.

South Korea

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

NIS-OKR-DUM-2009/1

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.