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Clinical and Functional Outcomes After Subtalar Arthroereisis in Pediatric Flexible Flatfoot

Baropodometric Evaluation After Subtalar Arthroereisis for Pediatric Flexible Flatfoot: An Observational Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07803341
Acronym
STA-PFF
Enrollment
25
Registered
2026-09-03
Start date
2026-04-13
Completion date
2027-01-31
Last updated
2026-09-03

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

Conditions

Pediatric Flexible Flatfoot

Brief summary

Flexible flatfoot is common in children and adolescents. In some patients, the condition remains painful or limits activity despite non-surgical treatment. Subtalar arthroereisis is a minimally invasive operation in which an implant is placed in the sinus tarsi to limit excessive foot pronation while preserving joint movement. This observational study follows children and adolescents who receive subtalar arthroereisis as part of their planned clinical care. Clinical status, standing foot radiographs, plantar-pressure distribution, and walking characteristics are assessed before surgery and six months after surgery. The study aims primarily to describe changes in dynamic plantar loading and walking parameters. Changes in clinical scores and radiographic alignment are assessed as secondary outcomes. No treatment is assigned for research purposes, and all surgical and postoperative decisions are made according to routine clinical indications.

Interventions

PROCEDURESubtalar Arthroereisis

A conical titanium implant is inserted into the sinus tarsi through a minimally invasive approach to restrict excessive subtalar pronation while preserving joint mobility. Implant size and position are assessed clinically and under fluoroscopic guidance. Additional soft-tissue or navicular procedures may be performed when clinically indicated, including gastrocnemius lengthening; excision or regularization of a symptomatic accessory or prominent navicular; posterior tibial tendon reinsertion or retensioning; or anterior tibial tendon tenosuspension according to the Young technique. These procedures are determined by clinical need and are not assigned by the study protocol.

Sponsors

University of Pavia
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to 18 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Step-Cycle DurationBaseline and 6 months after surgery
Ground-Contact DurationBaseline and 6 months after surgery
Double-Support DurationBaseline and 6 months after surgery
Step LengthBaseline and 6 months after surgery
Anteroposterior Talonavicular Coverage Angle Measured on Weight-Bearing Radiographs Using SynapseBaseline and 6 months after surgeryThe anteroposterior talonavicular coverage angle will be measured in degrees using the Synapse software on radiographic images. The measurement will be performed at baseline, before surgery (T0), and approximately 6 months after surgery (T1), in the operated foot. The change from baseline to 6 months after surgery will be evaluated.
Anteroposterior Talocalcaneal Angle Measured Using SynapseBaseline and 6 months after surgeryThe anteroposterior talocalcaneal angle will be measured in degrees using the Synapse software on radiographic images. The measurement will be performed at baseline, before surgery (T0), and approximately 6 months after surgery (T1), in the operated foot. The change from baseline to 6 months after surgery will be evaluated.
Lateral Meary's Angle Measured Using SynapseBaseline and 6 months after surgeryThe lateral Meary's angle will be measured in degrees using the Synapse software on radiographic images. The measurement will be performed at baseline, before surgery (T0), and approximately 6 months after surgery (T1), in the operated foot. The change from baseline to 6 months after surgery will be evaluated.
Lateral Calcaneal Pitch Measured Using SynapseBaseline and 6 months after surgeryThe lateral calcaneal pitch will be measured in degrees using the Synapse software on radiographic images. The measurement will be performed at baseline, before surgery (T0), and approximately 6 months after surgery (T1), in the operated foot. The change from baseline to 6 months after surgery will be evaluated.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 4, 2026