Clinical trial Recruiting at 1 site Observational Ages 45 and up Women only

Can a blood marker called lumican reveal hidden fragility in postmenopausal osteoporosis

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

Run by Kanuni Sultan Suleyman Training and Research Hospital · NCT07677072 · Data updated 2026-11-12

This study tests whether serum lumican levels can help identify hidden fragility risk in postmenopausal women beyond what bone density shows.

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Quick facts

Study typeObservational
Ages45 Years and up
SexWomen only
Enrollment98 (estimated)
SponsorKanuni Sultan Suleyman Training and Research Hospital
Academic / other
Drugs / interventionsdenosumab
Locations1 site (Küçükçekmece, Istanbul)
StatusRecruiting
StartedMay 15, 2026
Main results expectedDecember 1, 2026
Study endsDecember 1, 2026
Registry record updatedJune 30, 2026
Trial IDNCT07677072 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are postmenopausal women 45 and older undergoing routine osteoporosis workup at the hospital who consent to blood testing.

Probably not a fit

Findings may not apply to premenopausal women or those not undergoing standard osteoporosis assessments, and some patients may not show a relationship between lumican and fracture risk.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective observational study enrolling about 100 postmenopausal women undergoing routine osteoporosis evaluation. Researchers will measure serum lumican levels and compare them with bone mineral density, handgrip strength, FRAX fracture risk scores, and history of falls or fragility fractures. No treatment will be given; data will come from standard clinical assessments plus a blood test for lumican. The goal is to see if lumican can uncover fracture risk not captured by BMD alone. The study is conducted at a single center in Istanbul, Turkey.

Why it matters

Potential benefit: If successful, lumican testing could help identify women at higher fracture risk who might benefit from preventive measures.

How similar studies have gone: Previous research has explored biomarkers for bone health, but this study investigates lumican specifically as an additional indicator beyond BMD.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey
    Küçükçekmece, Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

  • Principal investigator: Dilek Ün oguzhanasiltürk, MD — Kanuni Sultan and Süleyman Training Resarch Hospital
  • Study coordinator: Dilek Ün Oğuzhanasiltürk, MD
  • Email: dilekunoguzhan@gmail.com
  • Phone: +90 5056367184

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.