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Effects of different treatment methods on clinical efficacy of moderate and severe bunion valgus patients

A retrospective study on the clinical efficacy and safety of different osteotomy methods for treating moderate and severe hallux valgus

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100042991
Enrollment
Unknown
Registered
2021-02-03
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hallux Valgus

Interventions

V-group:V-group
Z-group:Z-group

Sponsors

Department of Orthopedics, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients with successful bunions with joint preservation without postoperative complications; (2) Patients have no heart disease, central nervous system injury and other basic diseases; (3) No primary mental disorders and dementia disease; (4) Can consciously cooperate with the completion of cognitive function assessment; (5) Agree to participate in the study and sign the informed consent; (6) The follow-up time was >= 6 months, and the clinical data and follow-up data were complete.

Exclusion criteria

Exclusion criteria: (1) Patients with complications after the fusion of the first metatarsophalangeal joint; (2) Suffer from heart disease, central nervous system injury and other basic diseases; (3) Suffer from primary mental disorder and dementia disease; (4) Can not consciously cooperate with the completion of cognitive function assessment; (5) Do not agree to participate in this study; (6) The follow-up time was less than 6 months, and the clinical data and follow-up data were incomplete.

Design outcomes

Primary

MeasureTime frame
HV angle;IMA;

Countries

China

Contacts

Public ContactZhang Hui

West China Hospital, Sichuan University

zhanghuiwestchina@163.com+86 18980601437

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026