Modified Chevron osteotomy for moderate and severe hallux valgus

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100053993

Enrollment

Unknown

Registered

2021-12-06

Start date

2022-01-01

Completion date

Unknown

Last updated

2022-11-07

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

Conditions

Hallux valgus

Interventions

Experimental group:modified Chevron osteotomy

Control group:Traditional Chevron osteotomy

Eligibility

Sex/Gender

All

Age

16 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 16 to 70 years (patients over 60 years old cannot suffer from more than 3 kinds of complications of heart, lung, liver and kidney function at the same time), no gender restrictions; 2. In line with moderate to severe hallux valgus, hallux valgus orthopedic surgery is required; 3. The heart, lung, liver and kidney functions are basically normal, or can tolerate surgery after treatment; 4. The blood coagulation function is normal.

Exclusion criteria

Exclusion criteria: 1. Active or recent infection; 2. Relative contraindications such as severe osteoporosis and Charcot joint disease; 3. History of hallux surgery on the surgical side; 4. Those with related allergies or a history of severe allergies, and those with immunodeficiency.

Design outcomes

Primary

Measure	Time frame
Foot X-ray;	—

Countries

China

Contacts

Public ContactXie Meiming

The General Hospital of Western Theater Command, PLA

93319521@qq.com+86 13594291020

Outcome results

None listed

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