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Recruiting NCT03494374

The Effect of Orthosis and Exercise in Pes Planus

No phase Interventional Pes Planus

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: UCBL orthosis.
Who it may be relevant to
Registry conditions: Pes Planus. Basic parameters: 3 years — 10 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

There is no definite evidence for the conservative treatment of pes planus. We want to verify the combination efficacy of orthosis and toe walking exercise for the treatment of pes planus.

Detailed description

Observation cohort study

We prescribe UCBL orthosis and teach toe walking exercise. And we will check standing foot radiography (AP/Lateral) annually. And we will compare the changes of talometatarsal angle and calcaneal pitch angle.

Interventions

  • Device UCBL orthosis
    toe walking exercise

Primary outcome measures

  • TM angle [Time frame: through study completion, an average of 1 year]
Secondary outcome measures (1)
  • CP angle [Time frame: through study completion, an average of 1 year]

Eligibility criteria

Inclusion criteria

  • Clinically diagnosed with pes planus
  • Calcaneal pitch angle < 15 degree

Exclusion criteria

  • peripheral neuropathy
  • infection
  • rheumatoid arthritis
  • operation history

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

South Korea · 1 center
  • Seoul national university bundang hospital — Seongnam-si

Identifiers

NCT: NCT03494374 · B-1701/377-303

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗