CompletedNot Applicable

Minimally Invasive Distal Chevron in Comparison to the Reverdin-Isham Osteotomy for Hallux Valgus Correction

Austria50 participantsStarted 2018-12-01

Plain-language summary

This study analyses the Reverdin Isham procedure, which is the most popular minimally invasive surgical hallux valgus correction method and the minimally invasive chevron osteotomy, representing the standard technique of open surgery. It is hypothesized that the two techniques would show significant differences in regard to radiological outcome (Hypothesis 1), clinical outcome (Hypothesis 2) and development of radiological recurrence (Hypothesis 3).

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * patients after minimally invasive distal Chevron osteotomy for hallux valgus deformity with a Minimum follow up of 24 months * patients with informed written consent for being analyzed * patients, of whom radiographs are available from preoperative throughout the follow-up time of 24 months Exclusion Criteria: * patients under 18 years of age * pregnant patients, or women below the age of 50 ys, of whom the pregnancy status is not clear * patients with mental illness or patients, who cannot follow the required postoperative Treatment or controls * patients, who refuse to participate * patients, who are assigned to other clinical studies

What they're measuring

radiological outcome after minimally invasive Chevron osteotomy in comparison to the minimally invasive Reverdin-Isham method presented in literature

Timeframe: change from preoperative to 24 months postoperative (as it is presented in literature)

Trial details

NCT IDNCT04288297

SponsorDr.Gerhard Kaufmann

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2019-08-31

View on ClinicalTrials.gov More Hallux Valgus and Bunion trials