Comparison Of Outcomes After Knee Arthroplasty Using Posterior-Substituting Versus Cruciate-Retaining Prostheses
NCT ID: NCT06170931
Last Updated: 2024-12-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
24 participants
INTERVENTIONAL
2021-04-14
2024-07-01
Brief Summary
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Detailed Description
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As a result, although there is no clear study suggesting which design is better, research on this subject has increased recently. Our aim is to define the superiority of these two designs over each other.
Patients with the same stage of knee osteoarthritis in both knees were selected. Total knee arthroplasty was performed in the same session by making the appropriate design for the appropriate knee simultaneously. Preoperative and postoperative joint range of motion examinations were performed on both knees separately. WOMAC and OXFORD scores were examined separately for both knees.
Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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A knee of a patient with osteoarthritis of both knees
Posterior cruciate ligament protective approach in patients with knee osteoarthritis
posterior cruciate ligament-retaining prostheses
Posterior cruciate ligament protective approach in patients with knee osteoarthritis
The other knee of a patient with osteoarthritis in both knees
Posterior cruciate ligament transection approach in patients with knee osteoarthritis
posterior cruciate ligament-substituting prostheses
Posterior cruciate ligament transection approach in patients with knee osteoarthritis
Interventions
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posterior cruciate ligament-retaining prostheses
Posterior cruciate ligament protective approach in patients with knee osteoarthritis
posterior cruciate ligament-substituting prostheses
Posterior cruciate ligament transection approach in patients with knee osteoarthritis
Eligibility Criteria
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Inclusion Criteria
2. Patients with secondary osteoarthritis of both knees
Exclusion Criteria
2. Patients with secondary osteoarthritis in both knees and who underwent unilateral knee prosthesis
3. Patients with primary osteoarthritis in both knees and who underwent bilateral knee prosthesis in different sessions
4. Patients with secondary osteoarthritis in both knees and who underwent bilateral knee prosthetics in different sessions.
ALL
No
Sponsors
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Bezmialem Vakif University
OTHER
Responsible Party
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Locations
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Bezmialem Vakıf University
Istanbul, Fatih, Turkey (Türkiye)
Countries
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References
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Li N, Tan Y, Deng Y, Chen L. Posterior cruciate-retaining versus posterior stabilized total knee arthroplasty: a meta-analysis of randomized controlled trials. Knee Surg Sports Traumatol Arthrosc. 2014 Mar;22(3):556-64. doi: 10.1007/s00167-012-2275-0. Epub 2012 Nov 3.
Rossi R, Bruzzone M, Bonasia DE, Marmotti A, Castoldi F. Evaluation of tibial rotational alignment in total knee arthroplasty: a cadaver study. Knee Surg Sports Traumatol Arthrosc. 2010 Jul;18(7):889-93. doi: 10.1007/s00167-009-1023-6. Epub 2010 Jan 8.
Insall JN, Lachiewicz PF, Burstein AH. The posterior stabilized condylar prosthesis: a modification of the total condylar design. Two to four-year clinical experience. J Bone Joint Surg Am. 1982 Dec;64(9):1317-23. No abstract available.
In Y, Kim JM, Woo YK, Choi NY, Sohn JM, Koh HS. Factors affecting flexion gap tightness in cruciate-retaining total knee arthroplasty. J Arthroplasty. 2009 Feb;24(2):317-21. doi: 10.1016/j.arth.2007.10.022. Epub 2008 Oct 25.
Chalidis BE, Sachinis NP, Papadopoulos P, Petsatodis E, Christodoulou AG, Petsatodis G. Long-term results of posterior-cruciate-retaining Genesis I total knee arthroplasty. J Orthop Sci. 2011 Nov;16(6):726-31. doi: 10.1007/s00776-011-0152-1. Epub 2011 Sep 10.
Kim YH, Choi Y, Kwon OR, Kim JS. Functional outcome and range of motion of high-flexion posterior cruciate-retaining and high-flexion posterior cruciate-substituting total knee prostheses. A prospective, randomized study. J Bone Joint Surg Am. 2009 Apr;91(4):753-60. doi: 10.2106/JBJS.H.00805.
Other Identifiers
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IRB00013890
Identifier Type: -
Identifier Source: org_study_id