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Active, not recruiting Observational

Incidence of Fragility Fractures and Osteoporosis Screening in Chronic Stroke Patients

NCT06804252 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-12-10
Last updated
2025-02-05

Condition(s) studied

Chronic StrokeOsteoporosisFragility Fractures

Study summary

Stroke is a known risk factor for the development of osteoporosis, leading to an increased risk of falls and fractures. Several international studies have associated stroke with hip fractures, showing an odds ratio ranging between 1.5 and 4. The literature frequently indicates a lack of management for bone metabolism in patients following cerebrovascular events. This study aims to evaluate the incidence of osteoporosis and fragility fractures in patients with chronic stroke. A secondary aim is to assess whether patients have been adequately screened for bone metabolism following a cerebrovascular event. This study is designed as a prospective observational study. Patients aged over 65 years with chronic stroke are assessed at the U.O.C. of "Functional Recovery and Rehabilitation" at A.O.U.P. "P. Giaccone," Palermo. During the assessment, clinical and demographic data are collected, including details of the cerebrovascular event (location, hemorrhagic/ischemic, date), pre-event and post-event disability/autonomy (Rankin scale), presence of fractures (location and date) in the patient's medical history (pre and post-event), femoral and lumbar DEXA for osteoporosis evaluation, and DeFRA for assessing the 10-year risk of fragility fractures.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged 65 years and older * Diagnosed with chronic stroke * Able to provide informed consent * Willing to participate in follow-up assessments * Stable medical condition that allows participation in the study Exclusion Criteria: * Patients with acute stroke * Severe cognitive impairment that prevents informed consent * Other major illnesses affecting bone metabolism (e.g., severe renal disease) * Patients already undergoing treatment for osteoporosis * Patients with conditions that contraindicate DEXA scan

Primary outcome measure(s)

  • Evaluating the Incidence of Osteoporosis and Fragility Fractures in Chronic Stroke Patients — From enrollment to the end of treatment at 6 months
    The primary objective of this study is to evaluate the incidence of osteoporosis and fragility fractures in patients with chronic stroke.

Trial sites (1)

FacilityCityRegionStatus
A.O.U.P. P. Giaccone, Palermo, Italia 90127 Palermo Italia
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 NCT06804252 on ClinicalTrials.gov ↗ ← All trials in Italy