Comparing plate versus screw fixation for foot joint fusion
Calcaneocuboid Arthrodesis in Triple Arthrodesis by Plate Versus Screw: Randomized Controlled Trial
This study is testing whether using plates or screws to fix a foot joint fusion works better for adults with joint problems.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 3 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Asyut) |
| Trial ID | NCT06003296 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the clinical and radiological outcomes of two fixation methods—plate and screw—for calcaneocuboid arthrodesis in adults. The calcaneocuboid joint is often affected by conditions like osteoarthritis and trauma, and this procedure is typically performed alongside other rearfoot surgeries. The researchers hypothesize that plate fixation may provide better stability and ease of use compared to traditional screw fixation. By comparing these two methods, the study seeks to determine the most effective approach for achieving successful joint fusion.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 65 who require calcaneocuboid fusion for various indications.
Not a fit: Patients under 18 or over 65, those with acute fractures, infections, or other specific conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and pain relief for patients undergoing foot joint fusion.
How similar studies have performed: While the approach of comparing fixation methods is common, the specific focus on calcaneocuboid arthrodesis using these two techniques has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: all patients who will be operated by calcaneocuboid fusion for any indication age range 18-65 no paralytic patients Exclusion Criteria: * age \< 18 , \> 65 acute calcaneal fracture infection non union bone defect that need bone graft refusing to participate in the study neuropathic patients
Where this trial is running
Asyut
- Assiut University — Asyut, Egypt (Recruiting)
Study contacts
- Principal investigator: Abdelrazik Talaat — Assiut University
- Study coordinator: Abdelrazik Talaat
- Email: Abdelraziktalaat@med.aun.edu.eg
- Phone: 01015828696
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.