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Clinical Trials in Turkey / NCT05936814
Recruiting Observational

Adductor Ratio in Severe Varus Gonarthrosis

NCT05936814 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2021-12-01
Last updated
2023-07-11

Condition(s) studied

Osteoarthritis, KneeGenu VarumJoint Prosthesis; Complications

Investigational drug(s) / intervention(s)

total knee arthroplasty

total knee arthroplasty: cemented bicondylar PCL substituting total knee replacement

Study summary

The restoration of the joint line (JL) is essential for the proper functioning of Total Knee Arthroplasty (TKA). The exact position of JL can be determined using anatomical landmarks such as femoral condylar width (TEW), tibial tubercle, fibular head, and adductor tubercle during preoperative planning or intraoperatively. However, in cases of severe varus deformity in Type M gonarthrosis, it is unknown which method is most suitable for accurately determining the precise JL position. The aim of this study is to identify the most appropriate method for determining the JL position in Type M gonarthrosis. To achieve this goal, two groups of patients with Type 1A and Type M gonarthrosis will be compared by measuring preoperative values and comparing them with intraoperative reference values.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * 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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Keçiören SUAM Ankara Turkey (Türkiye) Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05936814 on ClinicalTrials.gov ↗ ← All trials in Turkey