CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 400 enrolled
Drug / intervention
Silicone Hydrogel 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.

Search/NCT01873846
NCT01873846N/ACompleted
CompareCT.gov

A Study to Evaluate the Product Performance of a New Silicone Hydrogel Contact Lens

Bausch & Lomb Incorporated·interventional·Posted Jun 10, 2013·Updated Jul 24, 2019

In Brief

A clinical study evaluating Silicone Hydrogel Contact Lens for Myopia. Completed, enrolled 400 participants across 1 site.

Detailed Summary

The objective of this study is to evaluate the product performance of a new silicone hydrogel soft contact lens when worn by current soft contact lens wearers on a daily wear basis.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJun 10, 2013
Enrollment StartApr 1, 2013
Primary CompletionMay 1, 2013
Study CompletionJul 1, 2013
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 13.1 years ago

Interventions

Silicone Hydrogel Contact Lensdevice