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EQUISOCK: New Antiequine

NCT07333768 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2026-04-28

No results posted yet for this study

Summary

The goal of this experimental study is to test the feasibility and validity of a new orthosis in patients with ankle lesions (external popliteal sciatic nerve or nerve injuries resulting in loss of ankle dorsiflexion) of both sexes and all ages. The main question it aims to answer is:Is the new orthosis a support for ankle stability??Does the new orthosis improve ankle function and patients' quality of life??The control group will be the subjects themselves when wearing their conventional ankle orthosis or without it. Participants must wear the new ankle orthosis for at least one month to assess the effectiveness of the orthosis and evaluate any changes that have occurred in the ankle joint and muscles.

Conditions

  • Ankle (Ligaments); Instability (Old Injury)
  • Ankle Equinus
  • Ankle Dorsiflexion

Interventions

DEVICE

EQUISOCK

Participants must wear the new ankle orthosis during assessments and in their daily lives for at least one month, which is the duration of the study.

DEVICE

Other ankle orthosis

Participants must wear the conventional ankle orthosis and without orthosis, during assessments and before wearing the new one

Sponsors & Collaborators

  • University of Salamanca

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-01
Primary Completion
2026-10-31
Completion
2026-12-31

Countries

  • Spain

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 NCT07333768 on ClinicalTrials.gov