Actively Recruiting
Registry for Breast Cancer Patients Receiving Adjuvant Hormone Blockade Tracking Bone Mineral Metabolism and Fracture Occurrence Sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna
Led by IRCCS Azienda Ospedaliero-Universitaria di Bologna · Updated on 2025-01-14
3000
Participants Needed
1
Research Sites
941 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are establishing a registry to include all patients treated with adjuvant hormone blockade for previous breast cancer. The goal is to study the trends in bone mass and how they relate to calcium metabolism markers, as well as the occurrence and frequency of fractures over time. This registry will support future studies focused on bone health in this patient population. Patients treated with adjuvant hormone blockade, such as aromatase inhibitors, GnRH analogs, or tamoxifen, for breast cancer will be enrolled in the registry. Inclusion is offered consecutively to patients diagnosed and evaluated at the Endocrinology Unit for Bone Mineral Metabolism, in coordination with Oncology referrals. The registry includes patients seen from January 1, 2015, with enrollment ending December 31, 2029. Follow-up for each patient may last up to 10 years, with registry updates continuing through December 31, 2039. Participants will have undergone bone density scans and blood tests related to mineral metabolism. Researchers will collect and monitor data on bone mass, calcium metabolism laboratory values, and fracture incidence throughout the study period, averaging 15 years. The long-term follow-up aims to provide valuable insights into bone health outcomes in breast cancer patients receiving hormone-blocking therapies.
CONDITIONS
Official Title
Registry of Adjuvant Hormone-blockade Breast Cancer Patients Evaluated for Bone Mineral Metabolism
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 218 years or older
- Currently undergoing adjuvant hormone blockade therapy (aromatase inhibitors, GnRH analogs, tamoxifen) for breast cancer referred by UO Oncology Zamagni
- Have had a bone density scan at UO Radiology Lovato
- Have had blood tests related to mineral metabolism
- Provided informed consent to participate
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, Bologna, Italy, 40138
Actively Recruiting
Research Team
U
Uberto Pagotto, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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