At a glance
ClinicalIndex Comparison RecordN/ACompleted· 20 enrolled
Drug / intervention
Lotrafilcon A test contact lens +2 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.
Ocular Comfort and OCT Observation of Post Lens Clearance and Ocular Tissue Compression
In Brief
A clinical study evaluating Lotrafilcon A test contact lens, Lotrafilcon A control contact lens, and 1 other intervention for Ocular Comfort. Completed, enrolled 20 participants across 1 site.
Detailed Summary
The purpose of this study was to compare the fit and comfort of two types of contact lenses.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOcular Comfort
CountriesUnited States
CollaboratorsBascom Palmer Eye Institute
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartAug 2011
First PostedAug 2011
Primary CompletionDec 2011
TodayJul 2026
First PostedAug 26, 2011
Enrollment StartAug 1, 2011
Primary CompletionDec 1, 2011
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 14.8 years ago
Interventions
Lotrafilcon A test contact lensdevice
Silicone hydrogel single vision, soft contact lens with alternate parameters
Lotrafilcon A control contact lensdevice
Silicone hydrogel single vision, soft contact lens
Ultra-High Resolution Optical Coherence Tomographer (OCT)device
Investigational, nonsignificant risk device for measuring post lens clearance and ocular tissue compression during contact lens wear