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In-Vivo Biomechanical and Functional Evaluation System of Total Hip Arthroplasty

In-Vivo Biomechanical and Functional Evaluation System of Total Hip Arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800020400
Enrollment
Unknown
Registered
2018-12-28
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

end-stage bone and joint disease

Interventions

normal:no treatment
direct anterior approach:THA by direct anterior approach
posterolateral approach:THA by posterolateral approach

Sponsors

Shanghai Jiaotong University Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients: 1. before THA, or 6 months to 1 year after THA; 2. achieve a good recovery after THA, be able to endure daily activities; 3. no complications; 4. agree to attend the research. Health volunteers: Been confirmed not any hip diseases by a surgeon and radiologist through MRI.

Exclusion criteria

Exclusion criteria: Patients: 1. unable tolerate X-ray; 2. no willing to attend the research; 3. restricting activities due to fracture, infection and etc.; 4. unable to cooperate with the research. Health volunteers: 1. injury or chronic pain in hip; 2. unable to complete all research procedures; 3. pregnant woman.

Design outcomes

Primary

MeasureTime frame
kinematic paradigm in hip;—

Countries

China

Contacts

Public ContactYunsu Chen

Shanghai Jiaotong University Affiliated Sixth People's Hospital

yschen2016@hotmail.com+86 18930177313

Outcome results

None listed

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