Collecting data for evaluating computer-aided detection in mammography
Data Collection for CAD Evaluation
Universitaire Ziekenhuizen KU Leuven · NCT01600144
This study is collecting mammography data from women to see how well a computer program can help detect breast cancer.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Sex | Female |
| Sponsor | Universitaire Ziekenhuizen KU Leuven (other) |
| Locations | 1 site (Leuven) |
| Trial ID | NCT01600144 on ClinicalTrials.gov |
What this trial studies
This study involves the collection of raw mammography data to evaluate the effectiveness of computer-aided detection (CAD) using VUCOMp software. It focuses on women who have undergone digital mammography imaging, aiming to gather comprehensive data for analysis. The observational nature of the study means that no experimental interventions are applied; instead, existing data is utilized to assess CAD performance. The findings could enhance the understanding of CAD systems in breast cancer screening.
Who should consider this trial
Good fit: Ideal candidates for this study are women who have recently undergone digital mammography imaging.
Not a fit: Men will not benefit from this study as they are excluded from participation.
Why it matters
Potential benefit: If successful, this study could improve the accuracy of breast cancer detection through enhanced CAD systems.
How similar studies have performed: Other studies have shown promise in using CAD systems for mammography, indicating that this approach has potential based on previous findings.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * women who underwent a digital mammography imaging Exclusion Criteria: * men
Where this trial is running
Leuven
- UZLeuven — Leuven, Belgium (RECRUITING)
Study contacts
- Principal investigator: Chantal Van Ongeval, MR,Phd — Universitaire Ziekenhuizen KU Leuven
- Study coordinator: Chantal Van Ongeval, MD,Phd
- Email: chantal.vanongeval@uzleuven.be
- Phone: (0)16343746
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Data Collection, data mammography