CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 362 enrolled
Drug / intervention
FID 120947A contact lens disinfecting solution +2 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.

Search/NCT01912768
NCT01912768N/ACompleted
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Clinical Evaluation of the Safety and Efficacy of FID 120947A Compared to a Marketed Lens Care Solution

Alcon Research·interventional·Posted Jul 31, 2013·Updated Jul 9, 2015

In Brief

A clinical study evaluating FID 120947A contact lens disinfecting solution, renu fresh multi-purpose solution, and 1 other intervention for Myopia and 3 related conditions. Completed, enrolled 362 participants.

Detailed Summary

The purpose of this study is demonstrate substantial equivalence of an investigational contact lens disinfecting solution to a commercially available contact lens solution in silicone hydrogel and soft contact lens wearers.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia, Astigmatism, Hyperopia, Refractive Error
Countries--
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJul 31, 2013
Enrollment StartDec 1, 2013
Primary CompletionMay 1, 2014
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 12.9 years ago

Interventions

FID 120947A contact lens disinfecting solutiondevice

Investigational 3% hydrogen peroxide solution intended for simultaneous cleaning, protein removal, disinfecting and storage of silicone hydrogel and soft contact lenses

renu fresh multi-purpose solutiondevice

Commercially available solution indicated for cleaning, removing protein deposits, rinsing, chemical disinfection, and storage of soft contact lenses

Soft contact lensesdevice

Commercially available soft contact lenses worn a minimum of 8 hours each day on a daily wear basis for the duration of the study (90 days). A fresh pair will be dispensed on Day 0, Day 30, and Day 60.