At a glance
ClinicalIndex Comparison RecordN/ACompleted· 82 enrolled
Drug / intervention
1 Day Acuvue Moistdevice
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.
Myopia Progression After Ceasing Myopia Control Contact Lens Wear
In Brief
A clinical study evaluating 1 Day Acuvue Moist for Myopia. Completed, enrolled 82 participants across 1 site.
Detailed Summary
This is a continuation study for subjects who were previously fit with test or control lenses; all will stop wearing their study lenses assigned in the previous study and will start to wear an FDA-approved marketed spherical soft contact lens.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartMar 2010
Primary CompletionOct 2011
First PostedApr 2013
TodayJul 2026
First PostedApr 11, 2013
Enrollment StartMar 1, 2010
Primary CompletionOct 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 13.2 years ago
Interventions
1 Day Acuvue Moistdevice
Lenses will be worn in a daily wear modality