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Evaluation of Software Generated Customized Foot Orthoses

NCT05462912 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-08-01

Study results available
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Summary

The purpose of this study is to determine whether custom-made foot orthoses generate a significant decrease in the perception of pain among individuals with foot pain and/or ankle pain.

Conditions

  • Arthropathy of Ankle or Foot

Interventions

DEVICE

custom foot orthotic

The goal of this study is to find out whether the use of software generated custom-made orthopedic foot orthoses improves pain in the long term.

Sponsors & Collaborators

  • Soleit

    collaborator UNKNOWN

  • University of California, Davis

    lead OTHER

Principal Investigators

  • Eric Giza, MD · UC Davis Orthopaedic Surgery

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-10-01
Primary Completion
2023-11-01
Completion
2023-11-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05462912 on ClinicalTrials.gov