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Clinical Trials in Turkey / NCT07518212
Active, not recruiting Observational

OST and MORES in Male Osteoporosis

NCT07518212 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-02-04
Last updated
2026-04-08

Condition(s) studied

Male Osteoporosis

Study summary

The aim of this study is to compare the Male Osteoporosis Risk Score and the Osteoporosis Self-Assessment Tool with the gold standard DEXA in determining the risk of osteoporosis in the lumbar and femoral regions in male individuals in the Turkish population, and to investigate their sensitivity and specificity in the first stage of screening for the detection of male osteoporosis.

Eligibility

Sex
MALE
Min age
50 Years
Max age
75 Years
Healthy volunteers
No
İnclusion criteria: * Men aged 50-75 * Patients who underwent imaging with the STRATOS DEXA device at Kayseri City Hospital Exclusion criteria: * Patients younger than 50 or older than 75 years of age * Patients with secondary osteoporosis * Female patients * Patients with uncontrolled severe comorbid conditions * Patients with a history of pathological fractures

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kayseri City Education and Research Hospital Kayseri Kayseri

More Kayseri City Hospital trials in Turkey

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 NCT07518212 on ClinicalTrials.gov ↗ ← All trials in Turkey