Randomized Controlled Trial of Internal Fixation Reconstruction With Stent Screw in the Treatment of Kummell's Disease

Osteoporotic Vertebral Compression Fracture Clinical Trial

Official title: Internal Fixation Reconstruction With Stent Screw VS Balloon Kyphoplasty in the Treatment of Kummell's Disease: a Double Blinded Randomized Controlled Trial

Status Not yet recruiting

Clinical Trial Summary

This study is a multicenter, prospective, double-blind, randomized controlled trial using a parallel two-arm design to investigate whether the postoperative 6-month quality of life, vertebral stability, complication of patients with osteoporotic vertebral compression fractures (Kummell's disease) are better with the use of stent screw internal fixation and percutaneous bone cement reconstruction technique compared to patients undergoing traditional percutaneous balloon kyphoplasty (BKP) for vertebral augmentation

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Fractures, Compression
• Osteoporotic Vertebral Compression Fracture
• Spondylosis

• NCT number: NCT06093087
• Study type: Interventional
• Source: Second Affiliated Hospital, School of Medicine, Zhejiang University
• Contact: Wanli Li, MD
• Phone: +86 13967116021
• Email: liwanli@zju.edu.cn
• Status: Not yet recruiting
• Phase: Phase 1/Phase 2
• Start date: January 1, 2024
• Completion date: September 1, 2027