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Comparison of Earlier functional recovery in total hip arthroplasty between the direct anterior approach and posterolateral approach: A Randomized Controlled Trial

Comparison of Earlier functional recovery in total hip arthroplasty between the direct anterior approach and posterolateral approach: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16010136
Enrollment
Unknown
Registered
2016-12-12
Start date
2016-12-12
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

Hip osteoarthritis, Necrosis of femoral head, DDH

Interventions

group A:DAA
group B:PLA

Sponsors

West China Hospital, Sichuan university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria were patients who underwent total hip arthroplasty with a diagnosis of osteoarthritis of the hip, femoral head necrosis(Ficat III to IV), Crowe Type 1 or 2 dysplasia,and willingness to comply with the study protocol.

Exclusion criteria

Exclusion criteria: A diagnosis of Crowe Type 3 or 4 dysplasia, previous hardware, BMI=30kg/m2, prior hip surgery, an inability to tolerate general anesthesia, an unwillingness to participate in the study

Design outcomes

Primary

MeasureTime frame
CK;ESR;IL-6;CRP;HGB;HCT;—

Countries

China

Contacts

Public ContactKang Pengde

West China Hospital, Sichuan University

kangpd@163.com+86 18980601953

Outcome results

None listed

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