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Clinical Trials in Turkey / NCT07677072
Recruiting Observational

Can Serum Lumican Level Identify a Hidden Fragility Phenotype Beyond Bone Mineral Density in Postmenopausal Women?

NCT07677072 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-05-15
Last updated
2026-06-30

Condition(s) studied

OsteoporosisPostmenopausal OsteoporosisFrailtyFragility Fractures

Study summary

Osteoporosis is a major cause of morbidity and fragility fractures in postmenopausal women. Bone mineral density (BMD) alone may not fully reflect fracture risk and skeletal fragility. Lumican, an extracellular matrix proteoglycan involved in collagen organization and musculoskeletal tissue homeostasis, has emerged as a potential biomarker for bone health. This prospective observational study aims to investigate the relationship between serum lumican levels, bone mineral density, muscle strength, and clinical fragility indicators in postmenopausal women. Approximately 100 participants will undergo routine osteoporosis assessment including DEXA, laboratory testing, FRAX evaluation, and handgrip strength measurement. The study will evaluate whether serum lumican levels can identify a hidden fragility phenotype beyond conventional bone mineral density measurements.

Eligibility

Sex
FEMALE
Min age
45 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Inclusion Criteria: * Female sex * Age 45 years or older * Postmenopausal status * Attendance at the Physical Medicine and Rehabilitation outpatient clinic * Undergoing routine bone mineral density (DEXA) assessment and osteoporosis laboratory evaluation * Ability and willingness to provide written informed consent Exclusion Criteria: Exclusion Criteria: * Premenopausal women * Secondary causes of osteoporosis (e.g., malignancy, advanced renal failure, severe liver disease, significant endocrine disorders) * Active infection or acute inflammatory disease * Major surgery within the previous 6 months * Neurological or muscular disorders that may significantly affect muscle function * Inability to comply with study procedures and assessments * Current treatment with medications that significantly affect bone metabolism, including bisphosphonates, denosumab, teriparatide, or other anti-osteoporotic agents * Refusal or inability to provide written informed consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey Küçükçekmece Istanbul Recruiting

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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 NCT07677072 on ClinicalTrials.gov ↗ ← All trials in Turkey