At a glance
ClinicalIndex Comparison RecordN/ACompleted· 196 enrolled
Drug / intervention
Lotrafilcon A 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.
Non-dispense Comfort Comparison of Two Silicone Hydrogel Lenses
In Brief
A clinical study evaluating Lotrafilcon A contact lens and Senofilcon A contact lens for Myopia. Completed, enrolled 196 participants.
Detailed Summary
The purpose of this study is to compare subjective responses to two contact lenses after 15 minutes of wear.
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 16, 2008
Enrollment StartNov 1, 2008
Primary CompletionDec 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 17.5 years ago
Interventions
Lotrafilcon A contact lensdevice
Investigational, silicone hydrogel, spherical, soft contact lens
Senofilcon A contact lensdevice
Commercially marketed, silicone hydrogel, spherical, soft contact lens