At a glance
ClinicalIndex Comparison RecordN/ACompleted· 75 enrolled
Drug / intervention
soft (hydrophilic) contact lensdevice
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.
Clinical Performance of Qualis Silicone Hydrogel Soft Contact Lens Over 3 Months of Daily Wear
In Brief
A clinical study evaluating soft (hydrophilic) contact lens for Refractive Errors. Completed, enrolled 75 participants across 3 sites.
Detailed Summary
Three-month, open-label, bilateral, parallel group, randomized, daily wear contact lens dispensing study.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Errors
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
First PostedMar 2020
Enrollment StartJul 2020
Primary CompletionJan 2021
TodayJul 2026
First PostedMar 4, 2020
Enrollment StartJul 1, 2020
Primary CompletionJan 28, 2021
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 6.3 years ago
Interventions
soft (hydrophilic) contact lensdevice
The intervention is a daily wear soft contact lens