Enrolling by invitation NCT07590882
Evaluation of Return to Sports Activity After Periacetabular Osteotomy: An Observational Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Correction Factor.
- Who it may be relevant to
- Registry conditions: Hip Surgeries, Hip Developmental Dysplasia. Basic parameters: 12 years — 40 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
This study aims to collect datas about patient who underwent periacetabular osteotomy
Detailed description
The aim of the study is to understant the long term effet of the periacetabular osteotomy in terms of pain relief, patient satisfaction and ability to return to sports
Interventions
- Procedure Correction Factor
periacetabular osteotomy
Primary outcome measures
- return to sport [Time frame: follow-up of 6 months]
Secondary outcome measures (2)
- failure rate [Time frame: follow-up of 6 months]
- level of pain post operative [Time frame: follow-up of 6 months]
Eligibility criteria
Inclusion criteria
- Patients of both sexes who underwent periacetabular osteotomy (PAO) at the sites of the Istituto Ortopedico Rizzoli (IOR) in Bologna (CORTI), Argenta, and Bagheria between 2017 and March 2025
- Postoperative follow-up ≥ 6 months
- Complete clinical and radiographic documentation available for retrospective analysis
- Willingness to participate in the study
- Age at the time of surgery between 12 and 40 years
Exclusion criteria
- Patients unable to provide informed consent, unable to understand and decide, or minors whose parents/legal guardians do not provide informed consent
- Patients with previous or ongoing oncological diseases, if associated with a potential impact on joint function or bone healing
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Italy · 1 center
- IRCCS Istituto Ortopedico Rizzoli — Bologna
Identifiers
NCT: NCT07590882 · PAO-R