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CompletedNCT07621328clubfootUpdated Jun 2, 2026

Outcomes of Eight-Plate Epiphysiodesis for Residual Clubfoot Deformities

An observational study in Clubfoot Deformity and Forefoot Adductus, sponsored by Cairo University. Completed at 1 site in Egypt. Open to participants aged 4 Years to 10 Years. Per ClinicalTrials.gov, last updated 2026-06-02.

Sponsored by Cairo University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
15
Ages
4 Years to 10 Years
Sex
All
01

Study summary

Purpose:

The purpose of this prospective clinical study is to evaluate the radiographic outcomes, effectiveness, and safety of lateral calcaneocuboid guided growth using an extra-periosteal tension-band plate (eight-plate) to correct residual forefoot adduction (often referred to as a "bean-shaped foot") in growing children with relapsed idiopathic clubfoot.

Condition and Intervention:

Residual forefoot adduction remains a challenging deformity following primary infant clubfoot treatment. While traditional management often relies on invasive double-column midfoot osteotomies-which carry risks of permanent joint stiffness, nonunion, and cartilage damage-this study investigates a minimally invasive alternative. Eligible pediatric patients (ages 4 to 10 years) with symptomatic, flexible or partially flexible residual forefoot adduction undergo temporary lateral calcaneocuboid epiphysiodesis using an extra-periosteal eight-plate and two cannulated screws.

Methodology \& Expected Outcomes:

Patients are clinically categorized into simple relapses (isolated, flexible forefoot adduction) and complex relapses (rigid deformities associated with hindfoot varus or equinus) to evaluate treatment efficacy across different deformity profiles. Radiographic parameters, including the anteroposterior talo-first metatarsal angle (T1MA), calcaneo-fifth metatarsal angle (C5MA), and the medial-to-lateral (M/L) column ratio, are tracked postoperatively every 3 months. The primary goal is to determine if restricting lateral midfoot column growth allows the shorter medial column to catch up proportionally, thereby restoring normal foot alignment and preserving joint range of motion without the morbidity of structural bone cuts. Patients are monitored for complications, such as hardware loosening, and are tracked long-term until definitive skeletal maturity.

Read the detailed description

Purpose:

The purpose of this prospective clinical study is to evaluate the radiographic outcomes, effectiveness, and safety of lateral calcaneocuboid guided growth using an extra-periosteal tension-band plate (eight-plate) to correct residual forefoot adduction (often referred to as a "bean-shaped foot") in growing children with relapsed idiopathic clubfoot.

Condition and Intervention:

Residual forefoot adduction remains a challenging deformity following primary infant clubfoot treatment. While traditional management often relies on invasive double-column midfoot osteotomies-which carry risks of permanent joint stiffness, nonunion, and cartilage damage-this study investigates a minimally invasive alternative. Eligible pediatric patients (ages 4 to 10 years) with symptomatic, flexible or partially flexible residual forefoot adduction undergo temporary lateral calcaneocuboid epiphysiodesis using an extra-periosteal eight-plate and two cannulated screws.

Methodology \& Expected Outcomes:

Patients are clinically categorized into simple relapses (isolated, flexible forefoot adduction) and complex relapses (rigid deformities associated with hindfoot varus or equinus) to evaluate treatment efficacy across different deformity profiles. Radiographic parameters, including the anteroposterior talo-first metatarsal angle (T1MA), calcaneo-fifth metatarsal angle (C5MA), and the medial-to-lateral (M/L) column ratio, are tracked postoperatively every 3 months. The primary goal is to determine if restricting lateral midfoot column growth allows the shorter medial column to catch up proportionally, thereby restoring normal foot alignment and preserving joint range of motion without the morbidity of structural bone cuts. Patients are monitored for complications, such as hardware loosening, and are tracked long-term until definitive skeletal maturity.

02

Conditions studied

  • Clubfoot Deformity
  • Forefoot Adductus

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Keywords

  • Clubfoot; Residual forefoot adduction; Guided growth; Eight-plate; Medial-lateral column ratio; Pediatric foot deformity.
03

In context

Clubfoot

79 studies on the registry are indexed under Clubfoot; 18 are open to participants now.

This study's enrollment of 15 is below the median of 55 across 29 observational studies indexed under Clubfoot.

Browse Clubfoot studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
4 Years to 10 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

diatric patients presenting with symptomatic, flexible or partially flexible residual forefoot adduction (the clinical "bean-shaped foot") who had failed prior conservative management following primary treatment for idiopathic congenital clubfoot. The study cohort was recruited from a tertiary pediatric orthopedic center and followed prospectively to evaluate the outcomes of lateral column growth modulation.

Inclusion criteria

the children's age should be from 4 to 10 years old. children with clubfoot who still had symptomatic residual forefoot adduction

Exclusion criteria

Exclusion Criteria:

  • patients who had dynamic forefoot adduction
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
15 participants (actual)
Patient registry
No

Groups and cohorts

  • Simple Relapse Subgroup

    Pediatric patients presenting with isolated, flexible residual forefoot adduction following primary infant clubfoot treatment. These patients do not exhibit rigid multi-planar deformities or associated significant hindfoot varus.

    Procedure: Lateral Calcaneocuboid Guided Growth (Eight-Plating)

  • Complex Relapse Subgroup

    Pediatric patients presenting with rigid midfoot residual adduction components accompanied by fixed hindfoot varus or fixed equinus deformities following primary infant clubfoot treatment

    Procedure: Lateral Calcaneocuboid Guided Growth (Eight-Plating)

Interventions

  • ProcedureLateral Calcaneocuboid Guided Growth (Eight-Plating)

    emporary lateral calcaneocuboid joint epiphysiodesis using a tension-band plate (eight-plate). Under fluoroscopic guidance, a 2 cm lateral longitudinal incision is made over the joint line, and the eight-plate is transfixed across the calcaneocuboid physis using two 3.5 mm cannulated screws to gradually restrict lateral column overgrowth and allow medial column alignment

  • ProcedureLateral Calcaneocuboid Guided Growth (Eight-Plating)

    lateral calcaneocuboid joint epiphysiodesis using a tension-band plate (eight-plate). Under fluoroscopic guidance, a 2 cm lateral longitudinal incision is made over the joint line, and the eight-plate is transfixed across the calcaneocuboid physis using two 3.5 mm cannulated screws to gradually restrict lateral column overgrowth and allow medial column alignment.

06

What researchers measure

Primary outcomes

  1. talo-first metatarsal angle (TM1A)

    measuring talo-first metatarsal angle (TM1A) pre and post

    Time frame: up to 24 months postoperatively (Final follow-up)

  2. the calcaneo-fifth metatarsal angle (CM5A)

    measuring angle the calcaneo-fifth metatarsal angle (CM5A)

    Time frame: 24 month

  3. the length of the medial and lateral column ratio

    Time frame: 24 month

07

Study locations

1 site
  • Cairo university
    Giza, Egypt
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07621328
Lead sponsor
Cairo University
Responsible party
Mohamed Sobhy Ali Hassan (NINMS, Cairo University) — Principal investigator
First posted
Jun 2, 2026
Start date
Jan 18, 2024
Primary completion
Jan 18, 2026
Completion
Jan 18, 2026
Last update
Jun 2, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2023. You cannot join it, but the record below documents what was studied.

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