Pilot Study of Percutaneous Correction of Hallux Valgus
NCT ID: NCT05880407
Last Updated: 2025-03-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
40 participants
INTERVENTIONAL
2022-02-22
2026-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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standard treatment
SERI osteotomy
SERI osteotomy
Correction of varus deformity of the 1st Metatarsal that is stabilized with Kirschnner wire
experimental treatment
percutaneous osteotomy according to Chevron
percutaneous osteotomy according to Chevron
Correction of varus deformity by osteotomy stabilization with 2 screws inserted via dorsal percutaneous accesses to the 1st Metatarsal.
Interventions
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SERI osteotomy
Correction of varus deformity of the 1st Metatarsal that is stabilized with Kirschnner wire
percutaneous osteotomy according to Chevron
Correction of varus deformity by osteotomy stabilization with 2 screws inserted via dorsal percutaneous accesses to the 1st Metatarsal.
Eligibility Criteria
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Inclusion Criteria
* HVA (hallux valgus angle): 20°-40°
* IMA (intermetatarsal angle): 10°-20°
Exclusion Criteria
* 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
* systemic pathologies that may impair bone consolidation
18 Years
65 Years
ALL
No
Sponsors
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Istituto Ortopedico Rizzoli
OTHER
Responsible Party
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Locations
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Istituto Ortopedico Rizzoli
Bologna, , Italy
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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hallux valgus
Identifier Type: -
Identifier Source: org_study_id
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