At a glance
ClinicalIndex Comparison RecordN/ACompleted· 84 enrolled
Drug / intervention
Multifocal Contact 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.
Accommodative Relief for Uncomfortable Non-Presbyopes
In Brief
A clinical study evaluating Multifocal Contact Lens and Single Vision Contact Lens for Asthenopia. Completed, enrolled 84 participants across 1 site.
Detailed Summary
This study will determine how multifocal contact lens correction affects symptoms of discomfort and asthenopia in a group of myopic contact lens wearers in the non-presbyopic age range (ages 30-40 years).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAsthenopia
CountriesUnited States
CollaboratorsBausch & Lomb Incorporated
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartFeb 2017
Primary CompletionMay 2018
First PostedJun 2018
TodayJul 2026
First PostedJun 1, 2018
Enrollment StartFeb 2, 2017
Primary CompletionMay 6, 2018
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 8.1 years ago
Interventions
Multifocal Contact Lensdevice
The multifocal contact lens (Bausch + Lomb ULTRA® for Presbyopia) will be worn for two weeks
Single Vision Contact Lensdevice
The single vision contact lens (Bausch + Lomb ULTRA®) will be worn for two weeks