At a glance
ClinicalIndex Comparison RecordN/ACompleted· 206 enrolled
Drug / intervention
LCS Complete Duofix +1 moredevice
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.
A Prospective, Randomised, Single Blinded Study Comparing the Pain, Biological Fixation and Outcomes of Patients With LCS Complete Duofix or LCS Porocoat Knee Systems
In Brief
A clinical study evaluating LCS Complete Duofix and LCS Complete Porocoat for Osteoarthritis. Completed, enrolled 206 participants across 1 site.
Detailed Summary
The primary objective of this investigation is to test the hypothesis that the Duofix Tibial component results in a reduction of immediate postoperative pain compared to the LCS Porocoat version.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOsteoarthritis
CountriesIreland
Collaborators--
Timeline
N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartSep 2006
First PostedAug 2008
Primary CompletionOct 2009
Study CompletionOct 2018
TodayJul 2026
First PostedAug 13, 2008
Enrollment StartSep 1, 2006
Primary CompletionOct 1, 2009
Study CompletionOct 22, 2018
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 17.9 years ago
Interventions
LCS Complete Duofixdevice
Orthopaedic implant for total knee replacement with Duofix biological fixation surfaces
LCS Complete Porocoatdevice
Orthopaedic implant for total knee replacement with Porocoat biological fixation surfaces