At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 40 enrolled
Drug / intervention
Synera +1 moredrug
Likely dose
Synera 70 mgfrom 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.
Efficacy and Safety of Synera in OA Pain
In Brief
A Phase 2 clinical trial evaluating Synera and Inactive patch for Knee Osteoarthritis. Completed, enrolled 40 participants across 1 site.
Detailed Summary
Knee osteoarthritis (OA) can result in significant pain and limitation of function. A number of topical non-steroidal anti-inflammatory drugs have been shown to reduce pain in this condition. This study examines a different topical approach, utilizing a topical anesthetic agent, to evaluate if application of such an agent would provide relief of exercise-induced knee pain in people with knee OA.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsKnee Osteoarthritis
CountriesUnited States
CollaboratorsNuvo Research Inc.
Timeline
Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJul 2012
Enrollment StartSep 2013
Primary CompletionSep 2014
Study CompletionFeb 2015
TodayJul 2026
First PostedJul 31, 2012
Enrollment StartSep 1, 2013
Primary CompletionSep 1, 2014
Study CompletionFeb 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 13.9 years ago
Interventions
Syneradrug
70 mg lidocaine/ 70 mg tetracaine topical patch applied once for 12 hours
Inactive patchdrug
placebo patch applied once for 12 hours