At a glance
ClinicalIndex Comparison RecordN/ACompleted· 60 enrolled
Drug / intervention
Lotrafilcon A Experimental Contact Lens +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.
Daily Wear Comparison of Enhanced and Non-Enhanced Silicone Hydrogel Lenses
In Brief
A clinical study evaluating Lotrafilcon A Experimental Contact Lens and Lotrafilcon A Commercial Contact Lens for Myopia. Completed, enrolled 60 participants.
Detailed Summary
The purpose of this study is to compare an experimental contact lens with a currently marketed contact lens.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartNov 2008
Primary CompletionDec 2008
First PostedDec 2008
TodayJul 2026
First PostedDec 23, 2008
Enrollment StartNov 1, 2008
Primary CompletionDec 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 17.5 years ago
Interventions
Lotrafilcon A Experimental Contact Lensdevice
Experimental spherical, silicone hydrogel soft contact lens
Lotrafilcon A Commercial Contact Lensdevice
Commercially marketed spherical, silicone hydrogel soft contact lens