Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07228611

Assesment and Comparison of Osteoporosis Risk Factors After Stroke

Comparison of Osteoporosis Risk in the Subacute and Chronic Periods Following Stroke and Evaluation of Factors Increasing Osteoporosis

Status
Recruiting
Phase
Study type
Observational
Enrollment
84 (estimated)
Sponsor
Ankara Etlik City Hospital · Other Government
Sex
All
Age
55 Years – 85 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to evaluate the effect of these factors and stroke itself on osteoporosis developing after stroke. Thus, the expected benefit of the study is to contribute to the identification and determination of the need for treatment in high-risk patients through further studies. There are no expected risks from the study.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTBone Mineral DensityPatients who have had a stroke and are at risk of fracture, and for whom routine assessment requires Bone Mineral Density (BMD) testing, will be included in the study. In addition, patients who have already undergone BMD testing for osteoporosis screening and who present to the outpatient clinic, with similar age and comorbidities, will be screened from the system, and 28 non-stroke patients who agree to participate will be included in the study.

Timeline

Start date
2025-12-05
Primary completion
2026-05-01
Completion
2026-05-01
First posted
2025-11-14
Last updated
2026-02-24

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07228611. Inclusion in this directory is not an endorsement.