At a glance
ClinicalIndex Comparison RecordN/ACompleted· 152 enrolled
Drug / intervention
lotrafilcon A contact lensdevice
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.
Clinical Evaluation of a Silicone Hydrogel Lens
In Brief
A clinical study evaluating lotrafilcon A contact lens for Myopia. Completed, enrolled 152 participants.
Detailed Summary
The purpose of this study is to assess the performance of an investigational contact lens among contact lens wearers.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartOct 2009
First PostedNov 2009
Primary CompletionDec 2009
TodayJul 2026
First PostedNov 18, 2009
Enrollment StartOct 1, 2009
Primary CompletionDec 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 16.6 years ago
Interventions
lotrafilcon A contact lensdevice
Investigational silicone hydrogel, single-vision, soft contact lens worn for four weeks at least as often as and on the same basis as participant's habitual lenses, as prescribed by participant's eye care practitioner -- ie., on a daily wear, flex wear, or extended wear basis.