At a glance
ClinicalIndex Comparison RecordN/ACompleted· 45 enrolled
Drug / intervention
senofilcon A +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.
Comparison of Two Marketed Lenses in a Controlled Environment
In Brief
A clinical study evaluating senofilcon A and lotrafilcon B for Eye Dryness. Completed, enrolled 45 participants across 1 site.
Detailed Summary
This study is comparing two silicone hydrogel contact lenses in a controlled environment for identification of characteristics associated to vision.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsEye Dryness
CountriesUnited Kingdom
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartJul 2014
First PostedAug 2014
Primary CompletionDec 2014
TodayJul 2026
First PostedAug 8, 2014
Enrollment StartJul 1, 2014
Primary CompletionDec 1, 2014
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 11.9 years ago
Interventions
senofilcon Adevice
Each study contact lens will be worn as daily wear modality for a period of 2 weeks each.
lotrafilcon Bdevice
Each study contact lens will be worn as daily wear modality for a period of 2 weeks each.