Flatfoot surgery holds up after a decade, small study suggests
NCT ID NCT07569835
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 20 people who had surgery as children to correct flatfoot. Researchers want to see if the correction lasts more than 10 years by checking foot structure and pain. They use simple tests like standing on tiptoes and X-rays to measure results.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- calcaneal stop and endorthesis (surgical implants)
- What this could lead to
- If successful, this could confirm that this surgery provides lasting correction of flatfoot in children, reducing the need for future treatments.
- What could go wrong
- This is a small, long-term follow-up study with only 20 patients, so results may not apply to everyone. Some patients may have pain or loss of correction over time.
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
-
About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
May 2024
- Expected to finish
-
May 2026
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
Primary objective: To evaluate, at more than ten years' follow-up, the clinical and radiological outcomes of patients who underwent subtalar arthroereisis with calcaneostop and endorthosis for the correction of pediatric flatfoot. Secondary objectives: To compare, within the same patient, the clinical and radiological outcomes of feet treated with subtalar arthroereisis using calcaneostop versus endorthosis.
- Ages
-
Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
-
Anyone
Show the full entry requirements Hide 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: Patients already in follow-up after undergoing subtalar arthroereisis with calcaneostop and endorthosis, enrolled in the study "Flatfoot treatment: comparison between resorbable endorthosis and resorbable calcaneal stop" by Prof. Giannini, still in follow-up at IOR. EXCLUSION CRITERIA: Patients who have undergone subsequent surgical procedures on the foot and ankle
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Flat foot acquired bilateral (pes planus) are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Istituto Ortopedico Rizzoli
RECRUITINGBologna, Italy
More trials for these conditions
Other studies related to the condition(s) this trial covers.