Pilot Study of Percutaneous Correction of Hallux Valgus
ConditionHallux Valgus
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorIstituto Ortopedico Rizzoli
About this trial
This is a pilot study with a randomized controlled design.
Eligibility criteria
Qualifiers
Patients of both sexes with adult hallux valgus with indication for corrective surgical treatment
HVA (hallux valgus angle): 20°-40°
IMA (intermetatarsal angle): 10°-20°
Disqualifiers
Patients with instability of the first metatarsophalangeal joint
Patients with severe morphostructural alterations or other pathologies in the foot and lower limb
patients requiring additional surgical procedures
patients with severe vascular and neurological systemic pathologies
Trial design
Treatments tested in this trial
- SERI osteotomy
- percutaneous osteotomy according to Chevron
Treatment groups
40 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov