At a glance
ClinicalIndex Comparison RecordN/ACompleted· 213 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.
Evaluation of Two Silicone Hydrogel Lenses Over a One Month Period
In Brief
A clinical study evaluating Lotrafilcon A contact lens and Comfilcon A contact lens for Myopia. Completed, enrolled 213 participants.
Detailed Summary
The purpose of this trial is to compare two different contact lenses during 4 weeks of wear.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartNov 2008
First PostedDec 2008
Primary CompletionJan 2009
TodayJul 2026
First PostedDec 18, 2008
Enrollment StartNov 1, 2008
Primary CompletionJan 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 17.5 years ago
Interventions
Lotrafilcon A contact lensdevice
Silicone hydrogel contact lens
Comfilcon A contact lensdevice
Silicone hydrogel contact lens