CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 35 enrolled
Drug / intervention
Tangible Boost +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/NCT03073148
NCT03073148N/ACompleted
CompareCT.gov

Evaluation of Tangible Boost Replenishing System

Tangible Science·interventional·Posted Mar 8, 2017·Updated Nov 17, 2020

In Brief

A clinical study evaluating Tangible Boost and Placebo saline for Contact Lens Solution. Completed, enrolled 35 participants across 1 site.

Detailed Summary

This study will evaluate Tangible Boost, a new contact lens care product which is designed to replenish the hydrogel layer on fluorosilicone acrylate lenses with Hydra-PEG. The Hydra-PEG coating is a poly(ethylene glycol)-based hydrogel that is covalently bound to the lens surface. This coating improves lens wettability, a common cause of patient discomfort. Tangible Boost is designed to maintain the wettability of Hydra-PEG lenses throughout the lens lifetime. Patients can use the Tangible Boost kit to reapply the Hydra-PEG coating each month at home.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsContact Lens Solution
CountriesUnited States
CollaboratorsUniversity of Houston

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedMar 8, 2017
Enrollment StartFeb 24, 2017
Primary CompletionFeb 13, 2019
TodayJul 2, 2026
Enrollment to primary: 2.0 yearsPosted 9.3 years ago

Interventions

Tangible Boostdevice

Participants will treat their lenses with Tangible Boost, a kit designed to maintain the wettability of Hydra-PEG treated fluorosilicone acrylate lenses.

Placebo salineother

Participants will treat their lenses with a placebo "Tangible Boost" kit, which contains saline in place of the Tangible Boost solution.