Actively Recruiting
Adductor Ratio Compared to Other Methods for Determining Joint Line in Severe Varus Gonarthrosis An Observational Study During Total Knee Arthroplasty Lead Sponsor: Saglik Bilimleri Universitesi
Led by Saglik Bilimleri Universitesi · Updated on 2023-07-11
68
Participants Needed
1
Research Sites
269 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the best way to restore the joint line (JL) during Total Knee Arthroplasty (TKA) for patients with severe varus deformity in Type M gonarthrosis, a form of knee osteoarthritis that causes pain and limited movement. The study compares two groups of patients with different types of gonarthrosis by measuring joint line positions before and during surgery to find the most accurate method. The aim is to improve knee function and reduce complications that can arise from incorrect joint line positioning, such as chronic pain and joint instability. The study involves patients undergoing cemented bicondylar posterior cruciate ligament (PCL) substituting total knee replacements. Researchers will use anatomical landmarks including the femoral condylar width, tibial tubercle, fibular head, and adductor tubercle to determine the joint line position. Preoperative X-rays and intraoperative caliper measurements will be taken, with follow-up X-rays after surgery. This approach seeks to validate the adductor ratio method as a reliable tool for joint line restoration, especially in cases with severe bone and cartilage damage. Participants will be monitored through preoperative, intraoperative, and postoperative assessments including imaging and functional evaluations over two years. The main outcome is the accuracy of joint line determination using the adductor ratio compared to other techniques. Researchers will track patient recovery and knee function to assess the effectiveness of the measurement methods. Safety and data completeness are also checked throughout the study period.
CONDITIONS
Official 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
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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
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