Clinical Trial

Bone Cement Augmented Transpedicular Screw Fixation Versus Cannulated Screws Fixation in Osteoporotic Spine

Recruiting
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Record status
This record was last updated December 23, 2025 (before its estimated June 1, 2026 completion). Its status may not reflect the trial's current state.
Summary
This study aims to compare the clinical and radiological outcomes of bone-cement-augmented transpedicular screw fixation versus cannulated pedicle screw fixation in patients with osteoporotic spines requiring posterior instrumentation, with respect to implant stability (loosening/pull-out), pain relief, functional recovery, and complication rates.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-12-06.
Status change: Not Yet Recruiting → Recruiting 2025-12-20
Trial Details
NCT Number NCT07294417
Lead Sponsor Kafrelsheikh University
Conditions Bone Cement Augmented Transpedicular Screw Fixation, Cannulated Screws Fixation, Osteoporotic Spine
Enrollment 70 participants
Start Date 2025-12-20
Primary Completion 2026-06-01 (estimated)
Study Completion 2026-06-01 (estimated)
Updated on ClinicalTrials.gov 2025-12-23