Actively Recruiting
The Adductor Ratio is More Reliable Than Other Techniques in Determining Joint Line in Severe Type M Varus Gonarthrosis
Led by Saglik Bilimleri Universitesi · Updated on 2023-07-11
68
Participants Needed
1
Research Sites
187 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating methods to accurately restore the joint line position during Total Knee Arthroplasty (TKA) in patients with severe varus deformity due to Type M gonarthrosis, a form of advanced knee osteoarthritis. This is important because proper joint line restoration affects knee function, pain, implant wear, and overall patient satisfaction. The study compares patients with two types of gonarthrosis deformities to find the best technique for determining the joint line using preoperative and intraoperative measurements, focusing particularly on the adductor ratio method. The study involves patients undergoing cemented bicondylar posterior cruciate ligament (PCL) substituting total knee replacement. Two patient groups include those with intraarticular varus deformity and those with metaphyseal varus deformity, both having severe osteoarthritis. Researchers will observe and measure anatomical landmarks during surgery and on radiographs before and after the procedure. This includes measuring the distance between specific bone landmarks and the joint line to assess which method most reliably determines the joint line position. Participants will undergo preoperative radiological assessments and intraoperative caliper measurements followed by postoperative X-rays over two years. Functional outcomes will be evaluated using the Hospital for Special Surgery (HSS) knee score before surgery and at one year after. The primary measurement is the accuracy of joint line determination by the adductor ratio compared to other techniques. This observational study aims to improve surgical planning and outcomes in complex knee replacement cases with severe deformity.
CONDITIONS
Brief Title
Adductor Ratio in Severe Varus Gonarthrosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 65 years of age
- Candidates with varus alignment osteoarthritis of the knee
- Patients with complete data set
- Patients who have agreed to participate in the study
You will not qualify if you...
- Patients who did not provide consent to participate in the study
- Patients with post-traumatic osteoarthritis
- Patients with inflammatory type of osteoarthritis
- Patients with incomplete data set
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day (surgery day)
Participants undergo cemented bicondylar PCL substituting total knee replacement surgery as part of their treatment for advanced knee osteoarthritis.
1 surgical visit (in-person)
Duration - Up to 2 years
Participants are monitored with repeated radiological measurements and functional assessments to evaluate joint line position and knee function over two years.
Periodic visits including preoperative, intraoperative, postoperative X-rays, and 12-month functional assessment
Trial Site Locations
Total: 1 location
1
Keçiören SUAM
Ankara, Turkey (Türkiye)
Actively Recruiting
Research Team
S
süheyla atay
B
bülent karslıoğlu
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here