Clinical Trials Logo
  1. Home
  2. Congenital Hip Dysplasia
  3. NCT02162186

Clinical and Radiographic Outcomes of the Corin Tri-Fit Total Hip Replacement

Avascular Necrosis Clinical Trial

Official title:
Analysis of Clinical Outcome and Implant Migration of the Cementless Tri-Fit Total Hip Replacement System

Clinical Trial Summary

The study will evaluate the radiographs (x-rays) of 100 patients with a TriFIT total hip at 2 weeks, 3 months, 6 months, 12 months, and yearly following surgery to see if there has been any movement or wear in the hip stem over the course of the study. The study will also record clinical data on each patient using various functional tests and questionnaires at the same intervals.

Clinical Trial Description

The present study will prospectively recruit 100 patients scheduled for elective total hip replacement with Corin's TriFIT Hip System at the Ottawa Hospital - General Campus. As part of their clinical care, patients routinely undergo a clinical examination and have had radiographs taken at 2 weeks, 3 months, 6 months, 12 months, and yearly following surgery. Using specialized software, radiographs from each interval will be examined to assess femoral stem migration and joint wear patterns. Femoral stem migration will be assessed using computer-assisted software. The study will also assess the rate of implant failure during the first two post-operative years. Clinical assessments and questionnaires will also be completed during each of the follow-up intervals. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02162186
Study type Observational
Source Corin
Contact
Status Completed
Phase
Start date October 2014
Completion date December 2019
View Details
See also
  Status Clinical Trial Phase
Active, not recruiting NCT03312465 - Anatomical Shoulder Domelock System Study
Completed NCT02139345 - TC-A Registration Study N/A
Completed NCT03540030 - Opioid-Free Shoulder Arthroplasty Phase 4
Completed NCT01285843 - Periprosthetic Bone Mineral Density After Total Hip Arthroplasty Performed Through a Minimally Invasive Anterior Approach (AMIS) With Either an AMIStem or a Quadra Femoral Component N/A
Completed NCT00750984 - A Comparison of Two Different Surgical Techniques for Total Hip Resurfacing N/A
Active, not recruiting NCT00175487 - Comparison of Hip Resurfacing to Large Femoral Head Total Hip Arthroplasty N/A
Terminated NCT00872547 - Multi-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and Primary Total Hip Replacement Phase 4
Completed NCT00603395 - A Prospective Clinical Study On A Total Hip Resurfacing System N/A
Recruiting NCT02503891 - AL-2 MP-1 (Polyimide) Acetabular Liner N/A
Completed NCT03666637 - Femoral Neck Fracture in Adult and Avascular Necrosis and Nonunion
Active, not recruiting NCT03343171 - Continuum Ceramic on Ceramic Bearing Post Market Clinical Follow-Up Study
Enrolling by invitation NCT05067543 - Perform Humeral System Study
Recruiting NCT05002335 - Clinical and Radiological Outcomes of Medacta Shoulder System (BE)
Active, not recruiting NCT03423953 - Comprehensive Nano - Post Market Clinical Follow-Up Study
Active, not recruiting NCT05049993 - Pyrocarbon Clinical Follow-up Study
Active, not recruiting NCT01700543 - Sidus(TM) Post Market Clinical Follow-up (PMCF) Study
Active, not recruiting NCT02199600 - The Medacta International GMK Sphere Post-Marketing Surveillance Study N/A
Not yet recruiting NCT01437124 - Metal Ions in Ceramic on Metal Total Hip Arthroplasty N/A
Terminated NCT00764959 - Retrospective Study of the Linear™ Hip Phase 4
Completed NCT00764673 - The 3DKnee™ System: A Post-Market Study Phase 4