Can a tiny foot implant reshape how children walk?

NCT ID NCT07803341

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time

Summary

This study follows children and teens with flexible flatfoot who are having a subtalar arthroereisis, a minimally invasive surgery that places a small titanium implant in the foot to limit excessive rolling inward. Researchers will measure foot pressure distribution, walking patterns, and foot alignment before surgery and six months after. The goal is to see how the procedure changes the way the foot contacts the ground and how the child walks. No treatment is assigned for research; all care follows routine clinical practice.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Subtalar arthroereisis, a minimally invasive procedure that places a small titanium implant in the foot to limit excessive rolling inward while preserving joint movement.
What this could lead to
If the procedure improves foot pressure and walking patterns, it could support its use as a treatment for painful or activity-limiting flatfoot in children.
What could go wrong
This is a small observational study, so it cannot prove cause and effect. The implant may not help all children, and surgery carries usual risks like infection or implant discomfort.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

25 people

The number who actually took part.

Started

Apr 2026

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Pediatric patients aged 10 to 18 years with symptomatic flexible flatfoot referred to the participating orthopedic unit and scheduled for elective subtalar arthroereisis after failure of appropriate conservative management or because of persistent symptoms, progressive deformity, or substantial functional impairment.

Ages

10 to 18 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Scheduled for elective subtalar arthroereisis, with or without adjunctive surgical procedures. * Aged 10 to 18 years at the time of enrollment. * Male or female. Exclusion Criteria: * Concomitant orthopedic or neurological conditions affecting walking ability. * Neurological or vestibular disorders affecting balance. * Contraindications to the medical devices used in the study. * Inability to understand and sign the informed consent form.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Pediatric flexible flatfoot are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Istituto di Cura Città di Pavia

    Pavia, Pavia, 27100, Italy