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Not yet recruiting NCT07449650

Calcaneal Lengthening Osteotomy With Locking Wedge Plate Versus Synthetic PEEK Cage Interposition for Symptomatic Flexible Pes Planovalgus Foot Deformity in Adolescents

No phase Interventional Flexible Flatfoot or Pes Planus

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: calcaneal lengthening osteotomy, calcaneal lengthening osteotomy with locking wedge plate, calcaneal lengthening osteotomy with synthetic PEEK cage interposition.
Who it may be relevant to
Registry conditions: Flexible Flatfoot or Pes Planus. Basic parameters: 10 years — 17 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this interventional study is to compare clinical outcome, radiological parameters, complication rates and time to recovery of calcaneal lengthening osteotomy with locking wedge plate versus PEEK cage interposition in management of symptomatic flexible pes planovalgus foot deformity in adolescents

Interventions

  • Procedure calcaneal lengthening osteotomy
    calcaneal lengthening osteotomy is a surgical procedure to correct symptomatic flexible pes planovalgus foot deformity in adolescents
  • Procedure calcaneal lengthening osteotomy with locking wedge plate
    one group will undergo calcaneal lengthening osteotomy with locking wedge plate fixation to maintain lengthening
  • Procedure calcaneal lengthening osteotomy with synthetic PEEK cage interposition
    second group will undergo calcaneal lengthening osteotomy with PEEK cage interposition to maintain lengthening

Primary outcome measures

  • Foot and ankle ability measure visual analogue scale radiological [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • patients with symptomatic flexible pes planovalgus indicated for surgical correction
  • age: from 10 years to 17 years
  • sex: males and females
  • failure of conservative management

Exclusion criteria

  • previous foot surgery
  • patients with neuromuscular disorders
  • patients with rigid pes Plano valgus
  • patients with sever comorbidities

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Sohag Faculty of Medicine — Sohag

Identifiers

NCT: NCT07449650 · Soh-Med-26-1-4MD

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗