New bunion surgery study tests faster recovery

NCT ID NCT03740282

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study follows 183 people aged 14 to 58 who had Lapiplasty surgery for bunions. The goal is to see if starting to walk within 3 weeks after surgery is safe and effective. Researchers will check if the bone heals properly and if the bunion comes back over 24 months.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Lapiplasty surgical procedure and device
What this could lead to
If successful, this could show that patients can safely bear weight sooner after bunion surgery, leading to faster recovery and fewer recurrences.
What could go wrong
This is a single-arm study without a comparison group, so results may not apply to all patients. Early weight-bearing could increase the risk of non-union or loss of correction.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

183 people

The number who actually took part.

Started

Nov 2018

Expected to finish

May 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

14 to 58 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Male and females between the ages 14 and 58 years at the time of consent * Closed physeal plates at the time of consent * Intermetatarsal angle is between 10.0 ̊ - 22.0 ̊ * Hallux valgus angle is between 16.0 ̊ - 40.0 ̊ * Willing and able to adhere to early weight-bearing instructions post-operatively * Capable of completing self - administered questionnaires * Acceptable surgical candidate, including use of general anesthesia * Female patients must be of non-child bearing potential or have a negative pregnancy test within 7 days prior to index procedure * Willing and able to schedule index procedure within 3 months of consent and able to return for scheduled follow-up visits * Willing and able to provide written informed consent Exclusion Criteria: * Previous surgery for hallux valgus on operative side * Previous surgeries on operative foot involving fusion of foot or ankle joints (other than hammertoe or lesser toes/digits) * Additional arthrodesis outside the first tarsometatarsal joint (other than: arthrodesis between the medial cuneiform and intermediate cuneiform and/or base of 2nd metatarsal; arthrodesis of hammertoe proximal interphalangeal joint or lesser toes/digits) * Moderate or Severe osteoarthritis of the MTP joint based on radiographic imaging (including lack of evident crista) or positive grind test * Symptomatic flatfoot or asymptomatic flatfoot (defined as calcaneal inclination \<5 ̊and talonavicular subluxation/uncovering \>50%) * BMI \>40 kg/m² * Current nicotine user, including current use of nicotine patch * Current clinical diagnosis of diabetes with fasting plasma glucose \> 126 mg/dL and/or HbA 1c ≥7.0 * Current clinical diagnosis of peripheral neuropathy or by assessment on 4 - point monofilament test * Current clinical diagnosis of fibromyalgia * Current clinical diagnosis of Complex Regional Pain Syndrome/Reflex Sympathetic Dystrophy (CRPS/RSD) * Current uncontrolled hypothyroidism * Previously sensitized to titanium * Currently taking oral steroids or rheumatoid biologics * Currently taking immunosuppressant drugs * Insufficient quantity or quality of bone to permit stabilization, conditions that retard healing (not including pathological fractures) and conditions causing poor blood supply such as peripheral vascular disease * Active, suspected or latent infection in the affected area * Use of synthetic or allogenic bone graft substitutes * Current diagnosis of metatarsus adductus (defined as MAA ≥ 23 ̊) * Scheduled to undergo a same - bilateral procedure. Patient agrees to refrain from the Lapiplasty® Procedure (or other hallux valgus procedures) on contralateral foot for minimum of 6 months post index procedure * Patient has previously been enrolled into this study for a contralateral procedure * Scheduled for any concomitant procedure that would alter patient's ability to early weight-bear post-procedure * Patient is actively involved with a workman's compensation case or is currently involved in litigation * Patient is currently or has participated in a clinical study in the last 30 days prior to signing * Patient has a condition or finding that, in the opinion of the Investigator, may jeopardize the patient's well-being, the soundness of this clinical study, or could interfere with provision of informed consent, completion of tests, therapy, or follow-up

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Bunion are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

ankylosis Bunion Hallux Valgus

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Desert Orthopaedic Center

    Las Vegas, Nevada, 89121, United States

  • Foot & Ankle Center of Iowa

    Ankeny, Iowa, 50023, United States

  • Foot & Ankle Center of Northern Colorado

    Greeley, Colorado, 80634, United States

  • Jefferson City Medical Group, P.C.

    Jefferson City, Missouri, 65109, United States

  • Stonebriar Foot & Ankle

    Frisco, Texas, 75034, United States

  • UT Southwestern

    Dallas, Texas, 75390, United States

  • University of Pennsylvania/Penn Medicine

    Philadelphia, Pennsylvania, 19106, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.