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NCT07045012

The Relationship Between Osteoporosis and Sarcopenia Parameters in Postmenopausal Women Under 60

Not yet recruiting Last updated 1 July 2025
What this trial tests

trial in Osteoporosis in 52 participants. Not yet recruiting.

Timeline
25 June 2025
Primary endpoint
25 July 2025
25 July 2025

Quick facts

Lead sponsorBeylikduzu State Hospital
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment52
Start date25 June 2025
Primary completion25 July 2025
Estimated completion25 July 2025

Conditions studied

Sponsor

Beylikduzu State Hospital

Who can join

Adults 50 to 59, female only, with Osteoporosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This cross-sectional study will include postmenopausal women under the age of 60 who visited the Physical Medicine and Rehabilitation outpatient clinic at Beylikdüzü State Hospital between June 25 and July 25, 2025. Participants must have undergone a bone mineral density (BMD) assessment within the past six months using Dual X-ray Absorptiometry (DXA). Both osteoporotic and non-osteoporotic patients will be enrolled. Sociodemographic data such as age, height, weight, and BMI will be recorded. Femoral neck and L1-L4 T-scores and BMD values will be obtained from existing DXA results. Information on osteoporosis treatment, presence of fecal incontinence, constipation, and medication use will be collected. In the second phase, sarcopenia will be assessed according to EWGSOP2 criteria using bioelectrical impedance analysis for skeletal muscle mass, handgrip strength, and the five-time sit-to-stand test. Differences between the osteoporotic and non-osteoporotic groups will be analyzed.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Osteoporosis

Currently open trials in the same condition.

Other Beylikduzu State Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07045012.

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