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Walking after foot surgery: can pressure patterns predict who needs extra help?

NCT ID NCT04823169

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
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early This study
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This status has not been confirmed recently, so it may be out of date.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 Jul 01, 2026 · Last updated Jul 02, 2026 · Updated 1 time

Summary

This study follows people who have had a type of minimally invasive foot surgery called DMMO to relieve painful metatarsalgia. Researchers measure foot pressure while walking at 7 and 30 days after surgery and track daily pain for a month. The goal is to see if early pressure patterns can predict which patients will need a custom foot orthotic three months later.

What this could mean

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

What this could lead to
If successful, this could help doctors predict which patients need extra support after foot surgery, potentially improving recovery and reducing long-term discomfort.
What could go wrong
This is a very small study with only 4 participants, so results may not apply to everyone. It is observational and does not test a new treatment.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

4 people

The number who actually took part.

Started

Sep 2022

Finished

Sep 2024

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.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Adult person * Affiliated or beneficiary of a statutory social insurance scheme * Free ans informed consent * Following foot surgery like DMMO only or DMMO and hallux valgus Exclusion Criteria: * Minor or legally protect adult * Amputation disturbing the natural course of the step * Osteoarticular diseases/sequelae affecting walking and/or balance * Neuromuscular diseases/sequelae affecting walking and/or balance * Vestibular disorders affecting balance * Patients requiring a walking aid (e.g., walker) * Pregnant woman * Patient with dementia who are unable to follow verbal instructions

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Centre Hospitalier Du Mans

    Le Mans, 72000, France