Long-term Survival of THA After Pelvic and/or Femoral Osteotomy

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorCentral Hospital, Nancy, France

About this trial

Analyze the long-term clinical and radiological outcomes of total hip arthroplasty (THA) in patients with hip dysplasia treated by pelvic osteotomy, femoral osteotomy, shelf acetabuloplasty, or a combination of these interventions, performed during childhood or early adulthood. The aim is to understand the impact of these early interventions on THA survival and long-term joint function.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients who underwent THA between 1998 and 2010 and had a prior surgical treatment for hip dysplasia (pelvic, femoral osteotomy, shelf acetabuloplasty or combined osteotomy)

Disqualifiers

None

Trial population

Male and female patients, with no age limit, operated in the Centre Chirurgical Emile Gallé, Nancy, France, between 1998 and 2010

Trial design

Design model

Case-only

Time perspective

Retrospective

Treatments tested in this trial

  • Total hip arthroplasty

    Procedure/Surgery

    Total hip arthroplasty

Treatment groups

20 Participants
are divided into 3 treatment groups
Group A: Pelvic osteotomy or shelf acetabuloplasty1 intervention
Group B: Femoral osteotomy1 intervention
Group C: Combined osteotomy1 intervention

Trial outcomes

Primary outcomes

1

survival

Study of 15 year survival of THA

Time frame
20 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: