Actively Recruiting
Bone Cement Augmented Transpedicular Screw Fixation Versus Cannulated Screws Fixation in Osteoporotic Spine
Led by Kafrelsheikh University · Updated on 2025-12-23
70
Participants Needed
1
Research Sites
23 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Bone Cement Augmented Transpedicular Screw Fixation Versus Cannulated Screws Fixation in Osteoporotic Spine
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 63;18 years old
- Both sexes
- Confirmed osteoporosis on DEXA scan with T-score 64; -2.5
- Painful osteoporotic vertebral fractures, degenerative instability, or traumatic compression fractures
- Unresponsive to conservative management and requiring surgical stabilization
You will not qualify if you...
- Healed or stable fractures responding to medical treatment
- Uncontrolled coagulopathy
- Active spinal infections such as discitis or osteomyelitis
- Spinal deformity exceeding 30 degrees
- Vertebral body collapse greater than 70 percent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kafrelsheikh University
Kafr ash Shaykh, Kafrelsheikh, Egypt, 33516
Actively Recruiting
Research Team
A
Ahmed A Zahra, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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