CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 60 enrolled
Drug / intervention
MINI MONOKA canalicular stent, 10 mm +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/NCT00743249
NCT00743249N/ACompleted
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A Three-Month Safety Study to Determine the Retention Times of Side-Arm Canalicular Stents

Alcon Research·interventional·Posted Aug 28, 2008·Updated Apr 4, 2013

In Brief

A clinical study evaluating MINI MONOKA canalicular stent, 10 mm and MINI MONOKA canalicular stent, 20 mm for Healthy and Dry Eye. Completed, enrolled 60 participants.

Detailed Summary

The purpose of this study was to determine the safety and retention times of two different lengths (10 mm and 20 mm) of the MINI MONOKA canicular stent when inserted in the eye for up to three months in subjects with or without dry eye.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy, Dry Eye
Countries--
Collaborators--

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedAug 28, 2008
Enrollment StartOct 1, 2008
Primary CompletionFeb 1, 2009
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 17.8 years ago

Interventions

MINI MONOKA canalicular stent, 10 mmdevice

40 mm hollow intubation stent composed of a silicon tube and an oval collarette head (plug), cut to 10 mm length

MINI MONOKA canalicular stent, 20 mmdevice

40 mm hollow intubation stent composed of a silicon tube and an oval collarette head (plug), cut to 20 mm length