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In vivo kinematic analysis of hindfoot joint using bi-plane fluoroscopy

In vivo kinematic analysis of hindfoot joint using bi-plane fluoroscopy - In vivo kinematic analysis of hindfoot

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000040167
Enrollment
22
Registered
2020-04-16
Start date
2020-04-17
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Osteoarthritis of ankle, avascular necrosis of the talus, talus fracture

Interventions

None listed

Sponsors

Chiba University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Two groups are set: patients who have undergone total ankle arthroplasty (patient group) and healthy individuals who have no history of ankle disease (healthy group). Patient group 1) Patients who have undergone total ankle arthroplasty at Chiba University Hospital, followed up at our outpatient clinic, and more than 6 months have passed since surgery 2) Patients who are over 20 years old at the time of obtaining consent 3) Patients who have received sufficient explanation for participation in this study, and who have fully understood and consented to the document by their own will. Healthy group 4) Those who have no history of disease on the target foot 5) Those who are 20 years of age or older when obtaining consent 6) A person who has received sufficient explanation for participation in this study, and who has obtained sufficient written consent from the person's free will.

Exclusion criteria

Exclusion criteria: Persons who falls under any of the following conditions are not included. Patient group 1) Patients who have difficulty walking alone 2) Patients who are judged inappropriate by the study investigator or the study coordinator for conducting this study safely Healthy group 3) Those who have limited range of motion or instability of the ankle joint, as revealed by an orthopedic surgeon 4) Those who have abnormalities such as ostheoarthritic changes in the ankle radiograph 5) Those who are judged inappropriate by the study investigator or the study coordinator for conducting this study safely

Design outcomes

Primary

MeasureTime frame
The range of motion and kinematic pattern of the hindfoot joint during dorsiflexion plantarflexion activities

Secondary

MeasureTime frame
Range of motion of hindfoot joints by manual examination SAFE-Q Radiographic measurements Implant size

Countries

Japan

Contacts

Public ContactYukio Mikami

Chiba University Hospital Orthopedics

deepdish20002000@yahoo.co.jp043-226-2117

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026