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Study identifier: NCT06486753 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

LSTR in Chevron Osteotomy

Condition: Bunion  ·  Sponsor: The Methodist Hospital Research Institute

PhaseNA
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to determine if performing a lateral soft tissue release during a Chevron osteotomy (or Akin osteotomy when appropriate) for bunions leads to better correction without added complications in 200 patients over the age of 18 years old with the capacity to consent and mild to moderate bunions that are determined to benefit from Chevron osteotomies by one of the IRB approved study physicians. The main questions it aims to answer are: How does the addition of a lateral soft tissue release (LSTR) in a Chevron osteotomy bunion surgery affect hallux valgus alpha angle (HVA) correction? How does the addition of an LSTR in a Chevron osteotomy bunion surgery affect intermetatarsal angle (IMA) degrees of correction? Researchers will compare Chevron osteotomy bunion surgeries with and without LSTR to see if LSTRs lead to better correction without added complications. Participants will: * Be randomized to a control group where they receive a typical Chevron osteotomy bunion surgery or to the experimental group where they receive a Chevron osteotomy bunion surgery with an LSTR. * Complete surveys preoperatively and at 3, 6, and 12 months after surgery. * Receive routine x-rays pre and postoperatively to compare hallux valgus angle (HVA).

This description comes directly from the study's public registry record.

Talk to the study team

Haley M Goble, MHA  ·  713-441-3930  ·  hmgoble@houstonmethodist.org

Always discuss trial participation with your own doctor first.

Locations (1)

Houston Methodist Research InstituteHouston, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06486753