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

NCT ID: NCT06959498

Last Updated: 2025-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

20 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-05-01

Study Completion Date

2025-06-01

Brief Summary

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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.

Detailed Description

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Conditions

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Hip Arthropathy Associated With Other Conditions Hip Dysplasia Survival, Prosthesis

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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Pelvic osteotomy or shelf acetabuloplasty

Total hip arthroplasty after pelvic osteotomy or shelf acetabuloplasty

Total hip arthroplasty

Intervention Type PROCEDURE

Total hip arthroplasty

Femoral osteotomy

Total hip arthroplasty after femoral osteotomy

Total hip arthroplasty

Intervention Type PROCEDURE

Total hip arthroplasty

Combined osteotomy

Total hip arthroplasty after a combination of pelvic osteotomy or shelf acetabuloplasty, and femoral osteotomy

Total hip arthroplasty

Intervention Type PROCEDURE

Total hip arthroplasty

Interventions

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Total hip arthroplasty

Total hip arthroplasty

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* 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)

Exclusion Criteria

\-
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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Olivier ROCHE

Dr

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Julia Richard

Role: CONTACT

+33628749343

Oliver Roche

Role: CONTACT

Other Identifiers

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2024PI083

Identifier Type: -

Identifier Source: org_study_id

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