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Study on joint capsule repair with synthetic mesh in patients at high risk of dislocation during hip arthroplasty

Study on joint capsule repair with synthetic mesh in patients at high risk of dislocation during hip arthroplast y

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046486
Enrollment
Unknown
Registered
2021-05-16
Start date
2021-05-15
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

Hip disease

Interventions

MESH group:The joint capsule was repaired with a patch
control group :Suture capsule

Sponsors

PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients undergoing primary hip arthroplasty; 2.Patients 18 years of age and older who are conscious; 3.Patients with advanced age, neuromuscular disease, connective tissue disease and other risk indicators for dislocation; 4.Physically and mentally healthy, patients are willing to participate in the study and sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. Infection at the surgical site of the hip joint; 2. Allergic to the mesh material in the test; 3. Patients with poor blood pressure or blood glucose control; 4. Poor compliance, unable to cooperate with the test; 5. Hemophilia, affected limb vascular disease; 6. Oral corticosteroids, immunosuppressant and other drugs.

Design outcomes

Primary

MeasureTime frame
Hip function score;The maximum internal rotation of the femur was 90 degrees below the hip flexion during the operation;—

Secondary

MeasureTime frame
Postoperative dislocation rate;Wound complications;Suture time;—

Countries

China

Contacts

Public ContactNi Ming

PLA General Hospital

niming301@163.com+86 13581915896

Outcome results

None listed

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