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ORLINT & ORLEXT: Orthosis for Knee

NCT07333911 · 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 lateral ligament knee lesions of both sexes and older than 18 years old. The main question it aims to answer is:

Is the new orthosis a support for knee stability?? Does the new orthosis improve knee function and patients' quality of life??

The control group will be the subjects themselves when wearing their conventional knee orthosis or without it.

Participants must wear the new knee orthosis for at least one month to assess the effectiveness of the orthosis and evaluate any changes that have occurred in the knee joint and muscles.

Conditions

  • Knee Brace
  • Knee

Interventions

DEVICE

Orlint-Orlext orthosis device

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

DEVICE

Conventional orthosis device

Participants must wear the conventional knee 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

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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

Countries

  • Spain

Study Locations

More Related Trials

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 NCT07333911 on ClinicalTrials.gov