drugset / Trial / NCT05058443

Denosumab and Osteoporotic Vertebral Compression Fracture

NCT05058443

Phase 2/3 Completed 90 enrolled Shenzhen People's Hospital
RandomizedParallel-groupDouble-blindTreatment

Summary

This study aimed to investigate the effect of denosumab on bone mineral density(BMD), bone turnover markers(BTMs), functional status, secondary fracture rate, and adverse effects in osteoporotic vertebral compression fracture (OVCF) patients after vertebroplasty during a 12-month follow-up period.

Timeline

Start
2020-01-06
Primary completion
2022-08-05
Completion
2022-08-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Denosumab Monoclonal antibody 60 mg Subcutaneous

Indications

No indication recorded.