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Clinical Trials in China / NCT05906147
Recruiting Observational

Health ImprOvement Program of Bone in China

NCT05906147 · tracked via the Priya Life Science China tracker
Sponsor
Second Xiangya Hospital of Central South University
Phase
Observational
Started
2021-02-27
Last updated
2023-06-15

Condition(s) studied

Osteoporosis

Investigational drug(s) / intervention(s)

Regular follow-up

Regular follow-up: Follow-up of the population was conducted to track the incidence of fractures

Study summary

Fracture risk factors have long been identified as key factors in osteoporosis and fragility fractures. The WHO recommended Fracture risk assessmenttool (FRAX) applies clinical risk factors to assess the absolute risk of osteoporotic fractures in each individual. Our preliminary study suggests that FRAX estimates may underestimate the risk of fractures in the Chinese population. In order to optimize the risk prediction model of osteoporotic fractures, a treatment threshold and its optimal cutting point were initially established based on the data of the health management Center of the Second Xiangya Hospital of Central South University.

Eligibility

Sex
ALL
Min age
40 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Dual-energy X-ray bone mineral density measurement was performed in the health management center of our hospital in the physical examination subjects over 40 years old. Have independent civil capacity and agree to participate, and sign informed consent Exclusion Criteria: * Under 40 years of age, Patients who had undergone hip replacement or lumbar surgery and could not perform dual-energy X-ray BMD testing; Patients who have been treated with effective anti-osteoporosis drugs or have a history of malignant tumors.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Health Management Center, The Second Xiangya Hospital of Central South University Changsha Hunan Recruiting

More Second Xiangya Hospital of Central South University trials in China

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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 NCT05906147 on ClinicalTrials.gov ↗ ← All trials in China