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NCT03073148 · ClinicalTrials.gov registry record · NA
Evaluation of Tangible Boost Replenishing System
A NA study of Contact Lens Solution, sponsored by Tangible Science.
- Completed
- Registry status
- NA
- Development phase
- 35
- Enrollment target
- 1
- Study location
NCT03073148 is a NA study of Contact Lens Solution that has completed, run by Tangible Science. The registered enrollment target is 35 participants. The trial reports 1 study location across 1 state.
The verdict
NCT03073148, a NA study of Contact Lens Solution, has completed, sponsored by Tangible Science.
- COMPLETED
- Registry status
- NA
- Development phase
- 35 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- DEVICE Tangible Boost
- OTHER Placebo saline
Study Locations (1)
Texas
- University of Houston - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2017-02-24 |
| Est. Completion | 2019-02-13 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03073148
The ClinicalTrials.gov registry entry for NCT03073148 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tangible Science, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Contact Lens Solution appearing as the primary indexed condition, and to 2 interventions - of which Tangible Boost is the first listed.
NCT03073148 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT03073148 about?
NCT03073148 is a clinical study titled "Evaluation of Tangible Boost Replenishing System". 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 impr...
What is the current status of trial NCT03073148?
This trial is currently completed. It is a NA study. The enrollment target is 35 participants. The study started on 2017-02-24. Estimated completion is 2019-02-13.
What conditions does trial NCT03073148 study?
This clinical trial studies the following conditions: Contact Lens Solution.
What interventions are being tested in trial NCT03073148?
The interventions under investigation include: Tangible Boost (DEVICE), Placebo saline (OTHER).
Who is sponsoring clinical trial NCT03073148?
This trial is sponsored by Tangible Science, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03073148 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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