CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 271 enrolled
Drug / intervention
Senofilcon C +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.

Search/NCT03351101
NCT03351101N/ACompleted

Clinical Study of Approved Contact Lenses

Bausch & Lomb Incorporated·interventional·Posted Nov 22, 2017·Updated Jan 8, 2021

In Brief

A clinical study evaluating Senofilcon C and Samfilcon A for Myopia. Completed, enrolled 271 participants across 11 sites.

Detailed Summary

Evaluation of Johnson \& Johnson Acuvue Vita (senofilcon C) soft contact lenses to the Bausch + Lomb Ultra (samfilcon A) soft contact lenses

Study Details

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

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedNov 22, 2017
Enrollment StartOct 23, 2017
Primary CompletionNov 10, 2017
Study CompletionDec 8, 2017
TodayJul 2, 2026
Enrollment to primary: 17 daysPosted 8.6 years ago

Interventions

Senofilcon Cdevice

Senofilcon C Contact Lens

Samfilcon Adevice

Samfilcon A Contact Lens