The reliability of a new guidance tool voor accurate cuppositioning in total hip arthroplasty

• Conditions: gewrichtskraakbeen; arthrosis; osteoarthritis; 10023213

• Registration Number: NL-OMON39661
• Lead Sponsor: Isala Klinieken

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 25

Inclusion Criteria

osteoarthritis of the hip

Exclusion Criteria

obesity
hip dysplasia
traumatic hip injury
patients with increased risk for infection

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>the difference of perioperative measured inclination and anteversion (by using<br /><br>the device) compared to the values calculated on CT.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>operating time, complications, such as: infection and pain at the entrancepoint<br /><br>of the markingpoint. </p><br>