At a glance
ClinicalIndex Comparison RecordN/ACompleted· 64 enrolled
Drug / intervention
Orion daily disposable 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.
A Two-Week Crossover Dispensing Evaluation Of Orion Daily Wear Soft Contact Lens
In Brief
A clinical study evaluating Orion daily disposable contact lens and Gemini daily disposable contact lens for Myopia. Completed, enrolled 64 participants across 1 site.
Detailed Summary
The primary objective of the study is to evaluate the clinical performance of test lens (Orion) in comparison with control lens (Gemini) over a period of two weeks of wear.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
202120222023202420252026
Enrollment StartSep 2020
First PostedOct 2020
Primary CompletionNov 2020
Study CompletionDec 2020
TodayJul 2026
First PostedOct 14, 2020
Enrollment StartSep 14, 2020
Primary CompletionNov 30, 2020
Study CompletionDec 31, 2020
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 5.7 years ago
Interventions
Orion daily disposable contact lensdevice
Subjects will be randomized to wear Orion lens for 2 weeks.
Gemini daily disposable contact lensdevice
Subjects will be randomized to wear Gemini lens for 2 weeks.