Skip to content

A clinical research of ankle fusion lengthening in the treatment of old fractures of the ankle joint

A clinical research of ankle fusion lengthening in the treatment of old fractures of the ankle joint

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004306
Enrollment
Unknown
Registered
2014-01-12
Start date
2014-02-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Old ankle joint fracture

Interventions

Experimental group:Ankle fusion lengthening
Control group:Ankle fusion of bone graft

Sponsors

Department of orthopedics, The Third affiliated Hospital of the Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. non operation treatment failure with severe joint dysfunction or intractable pain of arthritis of the ankle joint surface; 2. can not repair the severe ankle fractures; suppurative or tuberculous arthritis of the ankle; 3. avascular necrosis of talus or talus bone loss; 4. Charcot joint disease; 5. failed ankle replacement or first-time ankle failure of fusion; 6. equinus deformity; 7. not through internal or valgus osteotomy; 8. with neuropathy or damage due to paralysis of muscles, causing severe joint instability; 9. subjects guardians and / or subjects of voluntary informed consent, and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. adjacent hip and knee flexion contracture of 2 serious existence; 2. peripheral vascular disease operation cannot be improved; 3. peripheral joints (including the talonavicular joint, calcaneocuboid joint) serious degeneration of rheumatoid arthritis of the ankle; 4. associated with other diseases, researchers believe that will not be able to evaluate the curative effect and is unlikely to be completed is expected to follow-up patients the 5 researchers think; 5. do not have any suitable selected cases.

Design outcomes

Primary

MeasureTime frame
The AOFAS hindfoot score;Complication;

Secondary

MeasureTime frame
External fixation time;

Countries

China

Contacts

Public ContactWANG Ai-Ming

Department of orthopedics,The Third affiliated Hospital of the Third Military Medical University

trauma2@163.com+86 13308302730

Outcome results

None listed

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