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Clinical Trials/NCT04685239
NCT04685239
Not yet recruiting
Not Applicable

Risk of Dislocation After Total Hip Replacement: Dual Mobility Cup vs. Unipolar Cup. A Randomized Controlled Trial With Patients ≥65 Years Operated for Hip Osteoarthritis With Primary Total Hip Replacement (THR).

Northern Orthopaedic Division, Denmark1 site in 1 country1,000 target enrollmentApril 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dislocation, Hip
Sponsor
Northern Orthopaedic Division, Denmark
Enrollment
1000
Locations
1
Primary Endpoint
Early dislocation, Difference in dislocation within 1 year.
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

The general purpose of this study is to examine whether the dual mobility cup (Novae® Serf) reduces the number of hip dislocations after total hip replacement, both early dislocation (≤1 year) and late dislocation (>1 year) after primary THR compared with a conventional cup design (Trabecular MetalTM Modular Acetabular System).

Detailed Description

Surgery with THR for arthritis and other hip disorders has long been one of the most successful orthopedic surgical treatments. The majority of the patients gain pain relief and experience improved hip function. In 2017, a total of 10,691 THRs were implanted in Denmark (annual report 2018). Hip dislocation is a known complication after THR. It is a painful condition which may have far-reaching consequences for the patient, who may experience both physical and mental discomfort. Ultimately, multiple hip dislocations may result in reoperation. In the literature, the incidence of hip dislocation is reported at 2-6 %, and a more recent review reports a risk of 0.5-10 %. In Denmark, recurrent hip dislocation is the cause of 21 % of the reoperations per year according to The Danish Hip Arthroplasty Register. According to the British National Joint Registry (NJR) and the Australian register (AOANJRR), hip dislocation is the cause of 15.5 % and 21 %, respectively, of the reoperations. The best method to avoid reoperation due to instability is to choose the correct implant for the individual patient and thereby spare the patient of having to endure a painful complication and yet another procedure. There are multiple risk factors for instability after THR, and increased use of dual mobility cups (DMC) is already documented.

Registry
clinicaltrials.gov
Start Date
April 1, 2023
End Date
December 2035
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Northern Orthopaedic Division, Denmark
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with hip arthritis who are amenable to surgery with THR and age ≥ 65 years referred to the Department of Orthopedic Surgery at either Section Farsø, Frederikshavn Hospital or Aalborg University Hospital. Patients who are willing to participate in the trial and who give their written, informed consent after receiving oral and written information.

Exclusion Criteria

  • Patients who do not wish to participate.
  • Sequelae of Calvé-Legg-Perthes' disease, caput necrosis, epiphysiolysis.
  • Proximal femoral or acetabular fracture.
  • Hip dysplasia with subluxation Crowe types III and IV.
  • Earlier hip bone surgery (excluding arthroscopic surgery).
  • Elective bilateral surgery.
  • If the patient's bone morphology is unsuitable for a cemented Exeter® femoral stem.
  • Patients with no e-mail.

Outcomes

Primary Outcomes

Early dislocation, Difference in dislocation within 1 year.

Time Frame: 1 year after surgery

The primary outcome is the difference in cumulative incidence proportion of dislocation between the 2 randomized groups within the first year after total hip replacement. The information will be collected from both the patient through questionnaires and from the Danish Hip Arthroplasty Register and the Danish National Patient Register.

Secondary Outcomes

  • Difference in dislocation within 5 years(5 years after surgery)
  • Patient reported outcome measure: Oxford Hip Score (OHS)(1, 5 and 10 years)
  • Dislocation 10 year(10 years after surgery)
  • Patient reported outcome measure: European quality of life 5 dimensions (EQ-5D 5L)(1, 5 and 10 years)
  • Patient reported outcome measures: The Copenhagen Hip and Groin Outcome Score (HAGOS)(1, 5 and 10 years)
  • Prosthesis survival.(1, 5 and 10 year)

Study Sites (1)

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