CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 15 enrolled
Drug / intervention
NDE L68 StableFit® Punctal Plugdevice
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/NCT04280653
NCT04280653N/ACompleted
CompareCT.gov

An Open-Label, Multi-Center, Clinical Study Evaluating the Effect of the NDE L68 StableFit® Punctal Plug on the Tear Lake

Mati Therapeutics Inc.·interventional·Posted Feb 21, 2020·Updated Dec 8, 2020

In Brief

A clinical study evaluating NDE L68 StableFit® Punctal Plug for Dry Eye Syndromes. Completed, enrolled 15 participants across 2 sites.

Detailed Summary

To evaluate the effect of the NDE L68 StableFit® punctal plug on the tear lake.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDry Eye Syndromes
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedFeb 21, 2020
Enrollment StartAug 28, 2019
Primary CompletionDec 11, 2019
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 6.4 years ago

Interventions

NDE L68 StableFit® Punctal Plugdevice

Tear lake evaluation of the planned study eye, prior to insertion of the Punctal Plug and then tear lake evaluation at days 7 and 28 after punctal plug insertion.