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Recruiting Not applicable

Biomolecular Markers of Bone Metastasis

NCT06806462 · tracked via the Priya Life Science Italy tracker
Phase
Not applicable
Started
2024-09-17
Last updated
2025-02-04

Condition(s) studied

Bone Metastasis

Investigational drug(s) / intervention(s)

Biomolecular profile of bone metastases

Biomolecular profile of bone metastases: Describe the biomolecular profile of bone metastases

Study summary

The goal of this clinical trial is to characterize the biomolecular profile of bone metastases to define the predisposing profiles of bone metastasis, in patients with breast or lung or renal carcinomas or of the gastroenteric or prostate tract with bone metastasis.

The main question it aims to answer is:

Is it possible to predict the progression of bone metastasis by identifying biomarkers as risk factors for bone metastasis?

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \>= 18 years * Patients with breast or lung or renal or gastroenteric tract or prostate with bone metastases * Patients who knowingly express willingness to participate in the study after signing the written informed consent Exclusion Criteria: * None

Primary outcome measure(s)

  • Bone metastasis profiling — up to 100 weeks
    Characterizing the biomolecular profile of bone metastasis to define the predisposing profiles of bone metastasis. Transcriptional profile of * RANK/RANKL * OPG * PTHLH * IL-1/6/7/8/11, * TNF-alfa
  • Fracture pathological profiling — up to 100 weeks
    Characterizing the biomolecular profile of bone metastasis to define the predisposing risk profiles of fracture pathological. Fracture event yes/no and association with primary outcomes.

Trial sites (1)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna Bologna Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06806462 on ClinicalTrials.gov ↗ ← All trials in Italy