accuracy of a new tool for optimal placement of the acetabular component in Total Hip Arthroplasty

Withdrawn

• Conditions: degeneration of the hipjoint; osteoarthritis of the hip; 10023213

• Registration Number: NL-OMON34036
• Lead Sponsor: Isala Klinieken

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Withdrawn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

Inclusion Criteria

patients who signed the informed consent
patients who have symptomatic osteoarthritis of the hip and eligible for a total hiparthroplasty

Exclusion Criteria

standard contraindications, as prevailing for elective cemented total hip arthroplasty (infection, severe comorbidity of pulmonary, cardiac or metabolic nature).

Study & Design

• Study Type: Observational non invasive
• 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>