Clinical Trials Directory

Trials / Completed

CompletedNCT06950047

PediLoc® Blade Plate in Distal Femoral Osteotomies

Application of PediLoc®Locking Cannulated Blade Plate System in Distal Femoral Osteotomies - A Retrospective, Comparative Analysis of Consolidation Rates and Description of the Surgical Technique

Status
Completed
Phase
Study type
Observational
Enrollment
111 (actual)
Sponsor
University Children's Hospital, Zurich · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Background: The PediLoc® Locking Cannulated Blade Plate System, originally designed for proximal femoral osteotomies, has also been used for multidimensional deformity correction of the distal femur. This study describes the surgical technique and retrospectively analyses consolidation rates of distal femoral osteotomies using this system, comparing them to distal femoral osteotomies using the DePuy Synthes® 90°LCP Pediatric Condylar Plate. Materials and methods: A retrospective review was conducted for patients who underwent distal femoral osteotomy with the PediLoc® Blade Plate (Blade Plate) and the DePuy Synthes® 90°LCP Pediatric Condylar Plate (90°LCP-PCP) at the University Children's Hospital Zurich (2020-2024). Consolidation rates were assessed using Reborn-, Rust-, and modified Rust-scores at 6 weeks, 3 months, and 6 months postoperatively and compared using an unpaired t-test. Geometric planes of osteotomy were analysed, and a stepwise correction technique was described.

Conditions

Interventions

TypeNameDescription
PROCEDUREdistal femoral osteotomies using the PediLoc® Locking Cannulated Blade Plate Systemdistal femoral osteotomies using the PediLoc® Locking Cannulated Blade Plate System
PROCEDUREdistal femoral osteotomies using the 90°LCP-PCPdistal femoral osteotomies using the 90°LCP-PCP

Timeline

Start date
2025-03-28
Primary completion
2025-04-14
Completion
2025-04-14
First posted
2025-04-29
Last updated
2025-05-02

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT06950047. Inclusion in this directory is not an endorsement.