CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 169 enrolled
Drug / intervention
Lotrafilcon A 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/NCT00933166
NCT00933166N/ACompleted
CompareCT.gov

Assessing the Performance of Lotrafilcon A Lenses During a Three Month Period

CIBA VISION·interventional·Posted Jul 7, 2009·Updated Jul 10, 2012

In Brief

A clinical study evaluating Lotrafilcon A contact lens for Myopia. Completed, enrolled 169 participants.

Detailed Summary

The purpose of this trial is to assess the performance of an investigational contact lens over a three month period.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
Countries--
Collaborators--

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJul 7, 2009
Enrollment StartJun 1, 2009
Primary CompletionNov 1, 2009
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 17.0 years ago

Interventions

Lotrafilcon A contact lensdevice

Investigational silicone hydrogel, single vision, soft contact lens worn on a daily wear basis, flexible wear basis, or extended wear basis for three months