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Anterior Knee Pain Between Unisex Knee Prosthesis VS Gender Specific Knee Prosthesis Following MIS TKA

CompletedNot applicableNCT05045651
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Unisex knee prosthesis and patient specific knee prosthesis has the same anterior knee pain and patellar tracking

Study details

Official title
The Incidence of Anterior Knee Pain Between Unisex Knee Prosthesis and Gender Specific Knee Prosthesis Following Minimally Invasive Surgery Total Knee Arthroplasty: A Randomized Controlled Trial
Interventions
  • Procedure: Gender Solution®posterior stabilized NexGen® LPS Hi-Flex
  • Zimmer Biomet, Inc, Warsaw, IN, USA and standard posterior stabilized NexGen® LPS Hi-Flex
  • Zimmer Biomet, Inc, Warsaw, IN, USA
Sponsor
Thammasat University
Start date
2014-08-01
Primary completion
2018-07-01
Sex
Female
Age range
from 50 Years to 80 Years
Results posted
No results posted in this snapshot
Total sites listed
0

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: Aymptomatic knee OA with * varus deformity \< 30 degrees * range of motion \> 90 degrees * flexion contracture \< 20 degrees * recurvatum \< 20 degrees Exclusion Criteria: * gout * postraumatic arthritis * osteonecrosis of knee * inflammatory joint disease

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05045651