At a glance
ClinicalIndex Comparison RecordN/ACompleted· 17 enrolled
Drug / intervention
Sapphire 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.
A Contralateral Dispensing Clinical Trial of Study Test Silicone Hydrogel Lens Against Enfilcon A Silicone Hydrogel Lens
In Brief
A clinical study evaluating Sapphire Lens and enfilcon A for Myopia. Completed, enrolled 17 participants across 1 site.
Detailed Summary
This will be a 1-month dispensing, double-masked, randomized, contralateral study comparing the test lens against the control lens. The assignment of lenses to eyes (i.e. which lens type is to be worn in which eye throughout the study) will be selected according to a randomization table.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesCanada
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedSep 2015
Enrollment StartOct 2015
Primary CompletionDec 2015
Study CompletionApr 2016
TodayJul 2026
First PostedSep 2, 2015
Enrollment StartOct 1, 2015
Primary CompletionDec 1, 2015
Study CompletionApr 29, 2016
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 10.8 years ago
Interventions
Sapphire Lensdevice
Each subject randomized to wear either the test or control in either the left of right eye.
enfilcon Adevice
Each subject randomized to wear either the test or control in either the left of right eye.