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

Status: Recruiting
Location: See location...
Study Type: Observational
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
Participation Requirements
Sex: Female
Minimum Age: 45
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Turkey
Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
RECRUITING
Küçükçekmece
Contact Information
Primary
Dilek Ün Oğuzhanasiltürk, MD
dilekunoguzhan@gmail.com
+90 5056367184
Time Frame
Start Date: 2026-05-15
Estimated Completion Date: 2026-12-01
Participants
Target number of participants: 98
Treatments
Postmenopausal Women Undergoing Osteoporosis Evaluation
Postmenopausal women undergoing routine osteoporosis assessment will be included in this observational cohort. Participants will undergo bone mineral density measurement, routine osteoporosis laboratory evaluation, FRAX assessment, handgrip strength measurement, and serum lumican analysis. No treatment or interventional procedure will be administered as part of the study.
Sponsors
Leads: Kanuni Sultan Suleyman Training and Research Hospital

This content was sourced from clinicaltrials.gov