Foot and Ankle Arthrodesis or Osteotomy With Io-Fix Type Fixation

Not Applicable

Active, not recruiting

• Conditions: Foot and Ankle Arthrodesis; Foot and Ankle Osteotomy
• Interventions: Other: Follow-up of Io-Fix type fixation

• Registration Number: NCT04812353
• Lead Sponsor: Universitaire Ziekenhuizen KU Leuven

Brief Summary

The recovery of foot and ankle arthrodesis and osteotomy is still plagued by the problem of delayed consolidation or even pseudo-arthrosis. To date, the foot and ankle unit of UZ Leuven is using a state of the art system, called the Io-Fix system, to optimize the biomechanical stability.

However, the current literature lacks studies assessing and quantifying the advantages of the Io-Fix system. Objective presentations about the use of, and (early) results are currently missing. Therefore, the investigators want to take their responsibility to objectively investigate whether they can confirm and quantify the expected positive results of using the Io-Fix system. Subsequently, the investigators want to search for eventual unexpected problems with Io-Fix.

Detailed Description

The recovery of foot and ankle arthrodesis and osteotomy is still plagued by the problem of delayed consolidation or even pseudo-arthrosis. Some known risk factors for delayed consolidation are inherent to the patient and /or cannot be easily corrected by the surgeon: smoking, diabetes mellitus, use of NSAIDS, etc. Many other biological risk factors are well known. The fusion rate is one of these factors. This factor is influenced by the mechanical stability and compression at the level of arthrodesis. The right alignment till the moment of consolidation is an important factor as well.

Currently, two concepts leading to a better fusion rate are under investigation. First, research is done to optimize the local biological factors by using concentrated growth factors. Second, researchers are working towards optimal biomechanical stability and compression by further developing per-operative osteosynthesis material.

Following the optimal biomechanical stability concept, the following innovation was recently released: the Io-Fix system of Extremity Medical L.L.C. (Parsippany , NJ). This state of the art system has clear advantages compared to other systems. Based on the well-expected advantages, the Foot and Ankle unit of UZ Leuven has been using this system since more than one year. The initial subjective results with Io-Fix are strongly positive.

However, the current literature lacks studies assessing and quantifying the advantages of the Io-Fix system. Objective presentations about the use of, and (early) results are currently missing. Therefore, the investigators want to take their responsibility to objectively investigate whether they can confirm and quantify the expected positive results of using the Io-Fix system. Subsequently, the investigators want to search for eventual unexpected problems with Io-Fix.

However, the investigators believe that a larger study groups within a prospective framework with a longer follow-up is mandatory.

Study Timeline

• Study Start: 2014-04-01
• Study First Submitted: 2021-03-17
• Study First Submitted QC: 2021-03-22
• Study First Posted: 2021-03-23
• Status Verified: 2024-07
• Last Update Submitted: 2024-07-02
• Last Update Posted: 2024-07-03
• Primary Completion: 2025-12
• Study Completion: 2025-12

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 208

Inclusion Criteria

• Being routinely scheduled for a reconstructive surgical procedure for the following indications or involving the following type of procedure

  1. Any reconstructive procedure for Pes Planus, Pes Plano-valgus, or Posterior Tibial Tendon Dysfunction
  2. Tibio-talar arthrodesis or prosthesis
  3. Sub-talar -and/or (partial) Chopart - and/or Triple arthrodesis
  4. Pantalar arthrodesis with or without inclusion of the Chopart joint

Exclusion Criteria

• Age under 18

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Foot and ankle arthrodesis or osteotomy	Follow-up of Io-Fix type fixation	Patients who underwent a foot- or ankle reconstruction surgery using the Io-Fix system

Primary Outcome Measures

Name	Time	Method
Radiological and clinical evaluation	within a period of 1 year	Radiological and clinical evaluation will be combined to determine the fusion rate within a measured time span

Secondary Outcome Measures

Name	Time	Method
Short Form 36 Health Survey Questionnaire (SF-36)	within a period of 1 year	To capture patients' perceptions of their own health and well-being
American Orthopedic Foot and Ankle Score (AOFAS)	within a period of 1 year	To measure the outcome of treatment in patients who sustained a complex ankle or hindfoot injury

Trial Locations

Locations (1)

UZ Leuven; 🇧🇪 Leuven, Vlaams-Brabant, Belgium