At a glance
ClinicalIndex Comparison RecordN/ACompleted· 118 enrolled
Drug / intervention
Lotrafilcon A upgrade soft 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.
Assessment of Lotrafilcon A Contact Lenses
In Brief
A clinical study evaluating Lotrafilcon A upgrade soft contact lens for Myopia. Completed, enrolled 118 participants.
Detailed Summary
The purpose of this 3-month study is to evaluate subjective responses to an upgraded contact lens.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
Enrollment StartJul 2010
First PostedAug 2010
Primary CompletionDec 2010
TodayJul 2026
First PostedAug 20, 2010
Enrollment StartJul 1, 2010
Primary CompletionDec 1, 2010
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 15.9 years ago
Interventions
Lotrafilcon A upgrade soft contact lensdevice
Silicone hydrogel contact lens approved for daily wear and extended wear up to 30 consecutive nights.