Outcome comparison of minimally invasive total hip arthroplasty: A prospective random controlled trial based on patient administered self-evaluation indices

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900023227

Enrollment

Unknown

Registered

2019-05-17

Start date

2019-07-01

Completion date

Unknown

Last updated

2019-05-20

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

Conditions

Hip osteoarthritis, osteonecrosis of the femoral head, developmental dysplasia of the hip

Interventions

Group A:minimally invasive total hip arthroplasty

Group B:classical total hip arthroplasty

Eligibility

Sex/Gender

All

Age

30 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Osteoarthritis of the hip; 2.Femoral head necrosis(Ficat classification III~IV); 3.Developmental displasia of hip with osteoarthritis; 4.Primary total hip arthroplasty; 5.BMI<35kg/m2; 6.With willingness of comply with the study protocol.

Exclusion criteria

Exclusion criteria: 1.Patients with severe medical issues who can not tolerate general anesthesia; 2.Prior hip infections or surgery; 3.Patients undergone with hemiarthroplasties; 4.Patients with Obvious osteoporosis.

Design outcomes

Primary

Measure	Time frame
Timed-up-and-go;Timed-Stair-Climb;timed 25-m foot walk;	—

Secondary

Measure	Time frame
Short Form-36;Harris hip score;WOMAC score;Acetabulum inclination;Acetabulum anteversion;varus of femoral stem;	—

Countries

China

Contacts

Public ContactWang Changyao

The Affiliated Hospital of Qingdao University

swxg.1@163.com+86 18661807308

Outcome results

None listed

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