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

Foot and Ankle Arthrodesis or Osteotomy With Io-Fix Type Fixation : a Prospective Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04812353
Enrollment
208
Registered
2021-03-23
Start date
2014-04-01
Completion date
2021-09-24
Last updated
2026-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Foot and Ankle Arthrodesis, Foot and Ankle Osteotomy

Keywords

Arthrodesis, Osteotomy, Io-Fix system

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.

Interventions

OTHERFollow-up of Io-Fix type fixation

Follow-up of patients who underwent a foot- or ankle reconstruction surgery using the Io-Fix system

Sponsors

Universitaire Ziekenhuizen KU Leuven
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Radiological and clinical evaluationwithin a period of 1 yearRadiological and clinical evaluation will be combined to determine the fusion rate within a measured time span

Secondary

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

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 11, 2026