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HealthyNCT03272672

Effects of a Valgus Unloader Brace on Medial Femoral Cartilage

A study testing Össür Unloading Knee Brace in people with Healthy, run by University of North Carolina, Chapel Hill at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to determine the effect of a valgus unloader brace condition on the acute change in medial femoral condyle cartilage morphology using Ultrasound following a standardized walking protocol. Read more about this study

Who is it for?
Ages 18 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
Össür Unloading Knee Brace
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited States
Study dates
1 Sep 2017to 1 Nov 2019
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Uninjured participants. There will be no exclusion based on race, gender or ethnicity.

Who cannot join

  • congenital or degenerative joint condition, orthopedic implants, current joint pain (quantified as less than 2 on a 10cm visual analog scale),
  • cartilage injury of any joint, lower extremity fracture, or upper extremity fracture within the last year.
  • any major ligamentous or cartilage injury of the knee or hip joints, or reported of cartilage injury at the ankle.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of North Carolina at Chapel Hill

    Chapel Hill, North Carolina, 27599

Other trials in United States

About this study

Official title: Effects of a Valgus Unloader Brace on Medial Femoral Cartilage Changes Following Walking Protocol

The purpose of this study is to determine the effect of a valgus unloader brace condition on the acute change in medial femoral condyle cartilage morphology using Ultrasound following a standardized walking protocol.

Read the detailed description

Participants will report to an initial screening session during which knee alignment will be determined using a long-lever goniometer. For the assessment of baseline knee alignment, the participant will stand with feet facing forward directly underneath corresponding acromion processes and weight evenly distributed. The first axis will be measured from ASIS to midpoint of the patella and the second axis will be measured from the midpoint of the patella to the tibial tuberosity. The valgus angle will be used to determine eligibility for the study. To be eligible for this study, participants must present with a valgus knee alignment angle of ≥180° on the dominant limb defined as the limb the participant would use to kick a ball. Weight and height measurements will also be measured and used to calculate BMI. Once eligible, participants will determine a self-selected walking speed by walking between 2 sets of infrared timing gates (TF100, TracTronix). Starting approximately 5 steps before the first timing gate, participants will be instructed to walk at a speed described as "comfortable walking over a sidewalk". Each participant will complete 3 trials and the average walking speed will be calculated.

Pre-loading Protocol

Participants will report to the laboratory at the same time of day (±2 hours) for both sessions to account for diurnal variations within the cartilage. Upon arrival, participants will sit on a treatment table in the long-sit position with knees fully extended for 45 mins to allow time for cartilage reformation.

Ultrasonographic Assessment of the Femoral Articular Cartilage While seated with their back up against the wall, participants will flex their knee to 140° measured using a manual goniometer while. A measuring tape will be secured to the length of the table so that the position of the posterior calcaneus can be recorded to allow for consistent positioning across trials 15. A LOGIQe US system (General Electric Co., Fairfield, CT) with a 12MHz linear probe will be used to image both the medial and lateral femoral cartilage. The probe will be placed transversely in line between the medial and lateral femoral condyles just superior to the patella and rotated to maximize reflection off the articular cartilage. A transparent grid will be placed over the US screen to improve reproducibility of the US image. The midpoint of the intercondylar groove will be aligned with the center of the grid.

The level of the cartilage-bone interface at the edge of the image on either side will be recorded in order to ensure consistent positioning across US assessments. Three images will be collected of each knee at each time point. Following each loading condition, the participant will be placed in the same position as the pre-loading US assessment using the tape measure. Three images of the femoral cartilage will be recorded from each knee. All post-walking images will be captured within 5 minutes of the loading protocol.

Ultrasonographic Image Analysis All US images will be analyzed with the ImageJ software (National Institutes of Health, Bethesda, MD). Values for all measurement types will be obtained for each of the three images of the dominant limb at each time point (pre and post-walking) and averaged for statistical analysis.

Cartilage Thickness

Cartilage thickness (in millimeters) will be determined at the most inferior point of the intercondylar groove, the midpoint of the medial condyle, and the midpoint of the lateral condyle by drawing a line from the cartilage-bone interface to the synovial space-cartilage interface.

Cartilage Area The femoral cartilage will be divided into medial and lateral sections by identifying the midline at the most inferior point of the intercondylar groove. Each section of the cartilage will be outlined with a polygon function (Figure 1). The area (in square millimeters) of each section will be measured.

Average Cartilage Thickness The area (in square millimeters) of each section as determined in the cartilage area measure will then be divided by the length (in millimeters) of the section measured via a segmented line along the cartilage-bone interface (Figure 2). Average cartilage thickness (in millimeters) measures will be determined for the medial and lateral condyles. Values will be obtained for each of the three images per limb at each time point (pre and post-walking) and averaged for statistical analysis.

Cartilage Loading Protocol Immediately following pre-test ultrasound assessments, participants will be transferred from the table to a wheelchair in order to minimize knee loading not related to the walking condition. During the braced walking condition, a valgus unloader brace (Össür Unloader One®, Össur Americas, Orange County, CA) will be fitted by a certified athletic trainer per manufacturer instructions to the dominant limb while the participant is seated with knee flexed to approximately 80°.

The brace will be maximally adjusted to unload the medial compartment. The participant will take 30 steps to adjust to the brace. Adjustments will then be made as needed if the participant determines the fit is uncomfortable or too loose. The participant will take 30 more steps. Any final adjustments can be made at that point. The participant will then be transferred to and from the treadmill via wheelchair to control the amount of cartilage loading.

Control Protocol In the unbraced condition, the participant will repeat the brace protocol except that the participant will not be fitted with an unloader brace while seated. The participant will take 60 steps to keep the number of steps consistent across trials before being transferred to the treadmill. The participant will remain unbraced for the entire trial.

Loading Protocol Participants will maintain the self-selected walking speed for 5000 steps on a treadmill (4Front, WOODWAY, Waukesha, WI). Self-selected speed will be kept the same across both conditions. Participant will walk for 1 minute to adjust to treadmill. Steps will then be counted for 1 minute, and the time necessary to complete 5000 steps will be calculated (5000 divided by number of steps per minute).

Conditions
Healthy
Being tested
Össür Unloading Knee Brace

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Össür Unloading Knee BraceOther

    Also called Össür Unloader One®

    During the braced walking condition, a valgus unloader brace (Össür Unloader One®, Össur Americas, Orange County, CA) will be fitted by a certified athletic trainer per manufacturer instructions to the dominant limb while the participant is seated with knee flexed to approximately 80°.

    The brace will be maximally adjusted to unload the medial compartment.

Study groups in NCT03272672
Study groupRoleWhat they receive
BracedExperimentalÖssür Unloading Knee Brace used during walking protocol
Receives: Other: Össür Unloading Knee Brace
UnbracedNo interventionWalking protocol without the use of brace

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pre walking - Thickness (mm) of the Medial Femoral Articular Cartilage as measured by ultrasound

    Thickness of the articular cartilage on the Medial Femoral condyle will be measured in millimeters

    Measured: Prior to the walking protocol

  2. Post walking - Thickness (mm) of the Medial Femoral Articular Cartilage as measured by ultrasound

    Thickness of the articular cartilage on the Medial Femoral condyle will be measured in millimeters

    Measured: Immediately following the walking protocol (the post-test will be finished within approximately 5 minutes of concluding the walking protocol)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Sep 2017
  2. Study start1 Sep 2017
  3. Primary completion1 Nov 2019
  4. Study completion1 Nov 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03272672
Sponsor's protocol ID
17-0831
Status last verified
Mar 2020
First submitted
28 Aug 2017
Last updated
25 Mar 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Össür Unloading Knee Brace in people with Healthy, run by University of North Carolina, Chapel Hill at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Mar 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pre walking - Thickness (mm) of the Medial Femoral Articular Cartilage as measured by ultrasound (time frame: Prior to the walking protocol). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Mar 2020.

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