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Clinical Trial Summary

A case series to provide post marketing evaluation of the MyPAO surgical planning and patient specific guides technology. This will be a single-centre, multi-surgeon evaluation assessing the safety of the use of these guides in periacetabular osteotomy surgery.


Clinical Trial Description

After enrolment, baseline data will be collected including age, sex and ethnicity of the participant. The radiographic measures of centre edge angle of Wiberg and acetabular inclination will be measured by the surgeon and patient reported outcome measures (PROMS) will be collected. The PROMS collected at usual care timepoints in patients undergoing pelvic osteotomy will be collated for use in the dataset. Peri-operative data, including clinician opinion on ease of use, intraoperative dose of radiation used and device associated adverse events, will be recorded and reported in the results. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06037278
Study type Interventional
Source The Royal Orthopaedic Hospital NHS Trust
Contact
Status Recruiting
Phase N/A
Start date July 13, 2023
Completion date September 30, 2025

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