At a glance
ClinicalIndex Comparison RecordN/ACompleted· 266 enrolled
Drug / intervention
NexGen LPS-Flex Mobile Bearing Kneedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Prospective Multicenter Post Approval Study of the LPS-Flex Mobile Bearing Knee
In Brief
A clinical study evaluating NexGen LPS-Flex Mobile Bearing Knee for Osteoarthritis and 5 related conditions. Completed, enrolled 266 participants across 3 sites.
Detailed Summary
The purpose of the study is to assess the long-term performance of the NexGen LPS-Flex Mobile Bearing Knee in the treatment of patients with severe knee pain or degenerative knee disease.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOsteoarthritis, Traumatic Arthritis, Avascular Necrosis of the Femoral Condyle, Moderate Varus, Valgus, Flexion Deformities
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedMar 2009
Enrollment StartApr 2009
Primary CompletionJun 2020
Study CompletionJun 2021
TodayJul 2026
First PostedMar 3, 2009
Enrollment StartApr 1, 2009
Primary CompletionJun 1, 2020
Study CompletionJun 1, 2021
TodayJul 2, 2026
Enrollment to primary: 11.2 yearsPosted 17.3 years ago
Interventions
NexGen LPS-Flex Mobile Bearing Kneedevice
Total Knee Replacement