Evaluation of Return to Sports Activity After Periacetabular Osteotomy: An Observational Study
PAO-R
1 other identifier
observational
26
1 country
1
Brief Summary
This study aims to collect datas about patient who underwent periacetabular osteotomy
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Nov 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 4, 2025
CompletedFirst Submitted
Initial submission to the registry
April 30, 2026
CompletedFirst Posted
Study publicly available on registry
May 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2027
May 15, 2026
May 1, 2026
1.2 years
April 30, 2026
May 12, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
return to sport
The percentage of patients who return to their preoperative sports activity
follow-up of 6 months
Secondary Outcomes (2)
failure rate
follow-up of 6 months
level of pain post operative
follow-up of 6 months
Study Arms (1)
patient undergoing periacetabular osteootmy
patient undergoing periacetabular osteootmy
Interventions
Eligibility Criteria
patients undergoing periacetabular osteotomy
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
IRCCS Istituto Ortopedico Rizzoli
Bologna, 40136, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 30, 2026
First Posted
May 15, 2026
Study Start
November 4, 2025
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
January 1, 2027
Last Updated
May 15, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share