Effects of cancer treatments on metabolism and bone health in early breast cancer survivors

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to investigate the metabolic and bone health changes in post-menopausal women aged 50-70 who have been treated for early non-metastatic breast cancer. Over a five-year period, the study will assess factors such as bone mineral density, body composition, glucose metabolism, and nerve damage before and after chemotherapy. The goal is to identify the physiological and molecular mechanisms behind treatment-related side effects and to discover potential biomarkers for predicting and preventing metabolic diseases. A questionnaire will also be utilized to gather additional health information from participants.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Postmenopausal
* Breast cancer stage I-III
* Eligible to receive (neo-)adjuvant chemotherapy/other antineoplastic treatment

Exclusion Criteria:

* Prior malignancy
* Metabolic disease (diabetes mellitus etc)

Where it's running

• Rigshospitalet
  Copenhagen, Danmark, Denmark Recruiting

Study contacts

• Principal investigator: Peter Schwarz, Prof, MD — Copenhagen University Hospital, Rigshospitalet
• Study coordinator: Kristian Buch, cand.med.
• Email: buch.kristian@gmail.com
• Phone: 29434376

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.