Clinical-radiological outcome after periacetabular pelvic osteotomy (PAO) after Ganz with hip dysplasia

• Conditions: Q65.8; Other congenital deformities of hip

• Registration Number: DRKS00012815
• Lead Sponsor: Orthopädische Klinik der Medizinischen Hochschule im Diakovere Annastift

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-01-28
• Study Completion: 2020-02-27
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 73

Inclusion Criteria

Hip dysplasia with surgical treatment with PAO after Ganz
- Patient age over 18 years
- Full-range conversion surgery for hip dysplasia
- Follow up older than 24 months
- Age at the time of surgery between 16 and 55 years

Exclusion Criteria

- Advanced osteoarthritis (TONNES grade greater than or equal to 3) before surgical treatment with PAO to Ganz

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of pain:<br>The aim is to demonstrate the superiority of the periacetabular pelvic osteotomy (PAO) after Ganz compared to the surgery after Tönnies with reduction of the pain on the VAS scale by the value of 1.<br>For this purpose, the patients are written to, they receive the patient information and are asked to fill out the enclosed questionnaires. The patient fills out the VAS scale in comparison before surgery and now.

Secondary Outcome Measures

Name	Time	Method
The secondary Outcome is improved functionality, which should be demonstrated by the following clinical scores:<br>Harris Hip Score, HOOS Score, UCLA Activity Score<br>For this purpose, the patients are written to, they receive the patient information and are asked to fill out the enclosed questionnaires. The patient is asked to complete the Harris Hip Score, HOOS Score, and UCLA Activity Score for their pre-surgery condition and at the current time.